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Symptoms » Cleft lip » Glossary
 

Glossary for Cleft lip

Medical terms related to Cleft lip or mentioned in this section include:

  • 2q deletion: A rare chromosomal disorder where part of the long arm (q) of chromosome 2 is deleted resulting in various abnormalities which are determined by the size of the deleted portion.
  • 3q deletion: A rare chromosomal disorder where part of the long arm (q) of chromosome 3 is deleted resulting in various abnormalities which are determined by the size of the deleted portion.
  • 4p16.3 deletion: A rare genetic disorder where a portion of chromosome 4 is deleted at a location called 16.3. The condition is characterized by malformations in most parts of the body as the deletion affects growth and development of the fetus.
  • Aase Smith syndrome: A rare hereditary syndrome characterized by deformities such as cleft palate, joint contractures and hypoplastic anemia.
  • Aase Syndrome: A genetic condition which results in anaemia and some skeletal and joint deformities
  • Absent corpus callosum -- cataract -- immunodeficiency: A rare syndrome characterized by immunodeficiency, cleft lip or palate, cataract, reduced pigmentation and brain abnormalities.
  • Accutane -- Teratogenic Agent: There is strong evidence to indicate that the use of Accutane during pregnancy may cause a teratogenic effect on the fetus. A teratogen is a substance that can cause birth defects. The likelihood and severity of defects may be affected by the level of exposure and the stage of pregnancy that the exposure occurred at.
  • Achard syndrome: An inherited connective tissue disorder characterized primarily by a short head, long, slender bones, recessed lower jaw and loose hand and foot joints.
  • Acrocallosal Syndrome (Schinzel Type): A rare condition characterized by absence of portion of the brain (corpus callosum), mental deficiency, duplicated toes, mental deficiency and other abnormalities.
  • Acrofacial dysostosis atypical postaxial: A rare genetic disorder characterized by absence of some fingers and toes and characteristic facial features.
  • Acrofacial dysostosis autosomal recessive: A rare inherited disorder characterized mainly by facial, hand and foot anomalies. The disorder resembles Nager syndrome.
  • Acrofrontofacionasal dysostosis syndrome: A very rare syndrome characterized by abnormalities of the bones of the skeleton as well as mental retardation. Various facial, eye and urogenital anomalies are also present.
  • Alves Castelo dos Santos syndrome: A rare syndrome characterized by hair, eye, skin and spinal abnormalities.
  • Amphetamines -- Teratogenic Agent: There is strong evidence to indicate that the use of Amphetamines during pregnancy may cause a teratogenic effect on the fetus. A teratogen is a substance that can cause birth defects. The likelihood and severity of defects may be affected by the level of exposure and the stage of pregnancy that the exposure occurred at.
  • Ankyloblepharon filiforme adnatum -- cleft palate: A rare inherited genetic disorder characterized by a cleft palate and eyelid fusion.
  • Anophthalmia -- hypothalamo-pituitary insufficiency: A rare syndrome characterized mainly by small or absent eyes and malformations of the hypothalamus and pituitary gland.
  • Anophthalmia -- hypyothalamo-pituitary insufficiency: A rare syndrome characterized mainly by small or absent eyes and malformations of the hypothalamus and pituitary gland.
  • Anophthalmia cleft lip palate hypothalamic disorder: A very rare inherited disorder characterized by one missing eye and one very small eye, cleft lip, cleft palate and high levels of thyroid-stimulating hormone.
  • Anophthalmia plus syndrome: An extremely rare disorder characterized by absent or very small eyes, underdeveloped ears and other facial anomalies.
  • Apelt-Gerkin-Lenz Syndrome: A rare inherited syndrome characterized by clefting of the lip and palate as well as the absence of variable portions of all of the limbs.
  • Arthrogryposis distal type II: A very rare syndrome characterized by permanent flexion of the fingers as well as other birth defects.
  • Auricular abnormalities -- cleft lip with or without cleft palate -- ocular abnormalities: A rare syndrome characterized by the association of external ear and eye abnormalities, cleft lip and sometimes a cleft palate.
  • Auriculoocular anomalies -- cleft lip: A very rare syndrome characterized by the association of abnormal external ears and a cleft lip and sometimes a cleft palate. Only two cases of the condition has been reported.
  • Ausems Wittebol-Post Hennekam syndrome: A very rare syndrome characterized by the association of a cleft lip with retinal problems.
  • Autosomal Recessive Tetra-Amelia: A rare disorder characterized by the absence of all four extremities as well as skeletal, nervous system, craniofacial and other abnormalities. The condition is causes death before or soon after birth.
  • Axial mesodermal dysplasia spectrum: A variable range of defects that occur during fetal development. The defect occurs at a cellular level and affects the way various parts of the body develop.
  • BBB syndrome, X-linked: A rare genetic disorder characterized by defects along the midline of the body. The type and severity of symptoms can vary considerably. There are two subtypes of the disorder: type I is inherited in a X-linked manner and type II is inherited in an autosomal dominant manner. Females with type I tend to have few if any symptoms - often the only symptom is wide-set eyes.
  • Baraitser-Rodeck-Garner syndrome: A very rare syndrome characterized primarily by mental retardation, premature fusion of skull bones, kidney anomalies, seizures and facial anomalies.
  • Bartsocas Papa syndrome: A rare condition characterized by webbing of skin as well as various other physical and mental abnormalities.
  • Beemer-Langer syndrome: A very rare inherited condition characterized by a number of congenital abnormalities and death generally occurs during early infancy.
  • Birth defects: Conditions which are present at birth and are considered alterations to what is considered normal in a newborn baby
  • Bixler-Christian-Gorlin syndrome: A very rare syndrome characterized primarily by widely spaced eyes, small ears and a clefts in the lip, palate and nose.
  • Branchial clefts with characteristic facies, growth retardation, imperforate nasolacrimal duct: A rare genetic disorder characterized by branchial defects, tear duct obstruction and pseudocleft of the upper lip.
  • Branchial clefts with characteristic facies, growth retardation, imperforate nasolacrimal duct, and: A rare genetic disorder characterized by branchial defects, tear duct obstruction and pseudocleft of upper lip.
  • Branchio-Oculo-Facial Syndrome: A rare genetic disorder characterized by branchial defects, lacrimal duct obstruction and pseudocleft of upper lip.
  • Breath symptoms: Breath-related symptoms including breath odor
  • Breathing symptoms: Symptoms affecting the breathing systems.
  • Burn-McKeown syndrome: A rare genetic disorder characterized by choanal atresia (narrowing or blockage of nasal airway), deafness, heart defects and eye, ear and facial anomalies.
  • C-like syndrome: A rare disorder involving poor fetal growth, limb and facial defects and severe developmental delay.
  • CHARGE Syndrome: A rare disorder characterized by choanal atresia, coloboma, ear and genital abnormalities and congenital heart defects.
  • Camera-Marugo-Cohen syndrome: A rare syndrome characterized mainly by mental retardation, muscle weakness, obesity and an asymmetrical body.
  • Cardiac malformation, cleft lip-palate, microcephaly and digital anomalies: A newly described syndrome characterized by heart malformations, cleft lip/palate, small head and digital anomalies.
  • Cat Eye Syndrome: A rare chromosomal disorder involving abnormalities of chromosome 22 and characterized by coloboma of the iris, down-slanting palpebral fissures and anal atresia.
  • Catel-Manzke Syndrome: A rare genetic disorder characterized by a small jaw, cleft palate and an extra bone at the base of the pointer finger.
  • Cerebro-facio-thoracic dysplasia: A very rare syndrome characterized by mental retardation, spinal and rib defects and facial anomalies.
  • Cerebro-oculo-nasal syndrome: A rare syndrome characterized mainly by eye, nose and brain malformations.
  • Charlie M syndrome: A rare birth disorder characterized by facial abnormalities and malformed or missing parts of the ends of the arms and legs.
  • Choanal atresia -- deafness -- cardiac defects -- dysmorphism: A rare genetic disorder characterized by choanal atresia (narrowing or blockage of nasal airway), deafness, heart defects and eye, ear and facial anomalies.
  • Cholestasis -- pigmentary retinopathy -- cleft palate: A rare syndrome characterized by degeneration of retinal pigments, cleft lip, cleft palate, kidney problems and cholestasis (bile flow obstruction).
  • Chromosome 1, 1p36 deletion syndrome: A rare chromosomal disorder where deletion of a portion of chromosome 1 causes various abnormalities such as heart problems, mental retardation, developmental delay, facial dysmorphism and short stature. The symptoms are variable depending on the exact location of chromosomal deletion.
  • Chromosome 1, duplication 1p21 p32: A rare chromosomal disorder where duplication of a portion of chromosome 1 causes various abnormalities such as short stature, newborn or fetal death, small head, undescended testes and various facial abnormalities.
  • Chromosome 1, proximal deletion:
  • Chromosome 1, pter-p36: A very rare chromosomal disorder where the end portion of the short arm of chromosome 1 is missing. The type and severity of symptoms is variable.
  • Chromosome 1, uniparental disomy 1q12 q21: A rare chromosomal disorder where part or all of the short arm (p) of chromosome 1 is deleted resulting in various abnormalities which are determined by the size of the deleted portion.
  • Chromosome 10, Monosomy 10p:
  • Chromosome 10p deletion syndrome: A rare chromosomal disorder where there is a deletion of the short arm (p) of chromosome 10 resulting in variable abnormalities.
  • Chromosome 10p duplication/10q deletion syndrome: A rare chromosomal disorder where a section of the short arm (p) of chromosome 10 is duplicated and a section of the long arm (q) of chromosome 10 is deleted resulting in various abnormalities.
  • Chromosome 10p terminal deletion syndrome: A very rare syndrome caused by a chromosomal defect (10p terminal deletion) and can result in a variety of malformations that are similar to DiGeorge syndrome and velocardiofacial syndrome.
  • Chromosome 11q duplication syndrome: A rare chromosomal disorder where there are three copies of the long arm (q) of chromosome 11 rather than the normal two resulting in various abnormalities. The type and severity of symptoms depend on the amount and location of genetic material duplicated.
  • Chromosome 12p deletion: A rare chromosomal disorder where there is a deletion of the short arm (p) of chromosome 12 resulting in various abnormalities. The type and severity of symptoms varies depending on the amount and exact location of the genetic material that is deleted.
  • Chromosome 12p deletion syndrome: A rare chromosomal disorder where there is a deletion of the short arm (p) of chromosome 12 resulting in various abnormalities.
  • Chromosome 13 ring syndrome: A rare chromosomal disorder where genetic material from one or both ends of chromosome 13 is missing and the two broken ends have rejoined to form a ring. The resulting type and severity of symptoms is determined by the amount and location of genetic material missing.
  • Chromosome 13 trisomy syndrome: A rare chromosomal disorder where there are three copies of chromosome 13 rather than the normal two resulting in various abnormalities. Most die within months and there are few survivors after 10 years.
  • Chromosome 13q duplication syndrome: A rare chromosomal disorder where the long arm (q) of chromosome 13 is duplicated resulting in various physical, neurological and developmental abnormalities.
  • Chromosome 15q duplication syndrome: A rare chromosomal disorder involving an extra copy of genetic material from the long arm of chromosome 15. The type and severity of symptoms are determined by the amount and location of the duplicated genetic material.
  • Chromosome 15q, trisomy: A rare chromosomal disorder involving an extra copy of genetic material from the long arm of chromosome 15. The type and severity of symptoms are determined by the amount and location of the duplicated genetic material.
  • Chromosome 17q, partial duplication: A rare chromosomal disorder involving an extra copy of genetic material from the long arm of chromosome 17. The type and severity of symptoms are determined by the amount and location of the duplicated genetic material.
  • Chromosome 18 mosaic monosomy: An extremely rare chromosomal disorder where only some of the body's cells have one copy of chromosome 18 instead of the normal two. The severity and type of symptoms varies depending on how many and which body cells are affected.
  • Chromosome 1p deletion syndrome: A rare chromosomal disorder where part or all of the short arm (p) of chromosome 1 is deleted resulting in various abnormalities which are determined by the size of the deleted portion.
  • Chromosome 1q duplication syndrome: A rare chromosomal disorder involving duplication of the long arm (q) of chromosome 1 which results in various abnormalities depending on the size and location of the portion of duplicated genetic material.
  • Chromosome 2 trisomy syndrome: A rare chromosomal disorder where there are three copies of chromosome 2 instead of the normal two.
  • Chromosome 2, monosomy 2q: A rare chromosomal disorder where part of the long arm (q) of chromosome 2 is deleted resulting in various abnormalities which are determined by the size of the deleted portion.
  • Chromosome 21 monosomy: A rare chromosomal disorder where there is only one copy of chromosome 21 instead of the normal two leading to various abnormalities.
  • Chromosome 21q deletion syndrome: A rare genetic disorder where a portion of the genetic material from the long arm of chromosome 21 is missing. The symptoms or severity may vary somewhat between patients.
  • Chromosome 22, trisomy: A very rare disorder where there is an extra copy of chromosome 22 in all the body cells. The condition is usually fatal soon after birth or during the fetal stage.
  • Chromosome 22q deletion: A rare genetic disorder where a portion of the genetic material from the long arm of chromosome 22 is missing. The symptoms or severity may vary somewhat between patients.
  • Chromosome 22q deletion syndrome: A rare chromosomal disorder where the long arm of chromosome 22 is deleted resulting in various abnormalities.
  • Chromosome 3, trisomy 3p: A rare chromosomal disorder where a portion of the short arm (p) of chromosome 3 is duplicated so there is three copies of it rather than the normal two.
  • Chromosome 3, trisomy 3q: A rare chromosomal disorder where a portion of the long arm (q) of chromosome 3 is duplicated so there is three copies of it rather than the normal two. The condition is characterized by mental and growth deficiency, broad nose root and excessive hair growth.
  • Chromosome 3/B translocation: A rare chromosomal disorder involving a translocation of genetic material of chromosome 3.
  • Chromosome 4 short arm deletion: A rare chromosomal disorder where part or all of the short arm (p) of chromosome 4 is deleted resulting in various abnormalities which are determined by the size of the deleted portion.
  • Chromosome 4p deletion syndrome: A rare chromosomal disorder where part or all of the short arm (p) of chromosome 4 is deleted resulting in various abnormalities which are determined by the size of the deleted portion.
  • Chromosome 6, monosomy 6q: A rare chromosomal disorder where a part of the long arm (q) of chromosome 6 is deleted resulting in various abnormalities depending on the location and length of missing genetic material.
  • Chromosome 6p deletion syndrome: A rare chromosomal disorder where part or all of the short arm (p) of chromosome 6 is deleted resulting in various abnormalities which are determined by the size of the deleted portion.
  • Chromosome 6q deletion syndrome: A rare chromosomal disorder where a part of the long arm (q) of chromosome 6 is deleted resulting in various abnormalities depending on the location and length of missing genetic material.
  • Chromosome 7 deletion p15.1-p21.1: A chromosomal disorder where a small portion of chromosome 7 is deleted which results in a range of abnormalities.
  • Chromosome 7 ring syndrome: A rare chromosomal disorder where the ends of chromosome 7 have been deleted and the two broken ends have rejoined to form a ring shape resulting in a range of symptoms determined by the size of the genetic deletion.
  • Chromosome 7, monosomy 7q3: A very rare chromosomal disorder involving a deletion of material from chromosome 7 at a location known as q3 which results in a wide range of abnormalities.
  • Chromosome 7q partial deletion: A rare chromosomal disorder involving deletion of the long arm (q) of chromosome 7 which results in various abnormalities depending on the size and location of the portion of deleted genetic material.
  • Chromosome 8 recombinant syndrome: A rare recombinant chromosomal disorder involving chromosome 8 which results in various abnormalities.
  • Chromosome 9 trisomy syndrome: A rare chromosomal disorder where there are three copies of chromosome 9 in the body's cells instead of the normal two resulting in various abnormalities.
  • Chromosome 9, Tetrasomy 9p: A rare chromosomal disorder where there is four copies of the short arm of chromosome 9 instead of the normal two resulting in various abnormalities.
  • Chromosome 9, Trisomy 9p (Multiple Variants): A rare chromosomal disorder characterized by mental retardation, head and face malformations and various other abnormalities.
  • Chromosome 9, trisomy: A rare chromosomal disorder where there are three copies of chromosome 9 in the body's cells instead of the normal two resulting in various abnormalities. The type and severity of symptoms varies depending on the amount and exact location of the genetic material that is duplicated.
  • Chromosome 9p tetrasomy syndrome: A rare chromosomal disorder where there is four copies of the short arm of chromosome 9 instead of the normal two resulting in various abnormalities.
  • Cleft Palate and Cleft Lip: A condition involving the association of a cleft lip with a cleft palate.
  • Cleft lip -- palate -- abnormal thumbs -- microcephaly: A very rare syndrome characterized by a small head, thumb abnormalities and a cleft lip and palate.
  • Cleft lip -- palate -- ectrodactyly: A very rare syndrome characterized by a cleft lip and palate and missing fingers and toes.
  • Cleft lip -- palate -- mental retardation -- corneal opacity: A very rare syndrome characterized mainly by mental retardation, cleft lip and palate and cloudy corneas.
  • Cleft lip and palate -- malrotation -- cardiopathy: A very rare syndrome characterized by heart defects, malrotated intestines and various facial anomalies.
  • Cleft lip palate -- deafness -- sacral lipoma: A very rare syndrome characterized mainly by an opening in the palate and lip, deafness and a lipoma in the end portion of the spine.
  • Cleft lip palate -- oligodontia -- syndactyly -- pili torti: A very rare syndrome characterized by a cleft lip and palate, webbed fingers, missing teeth and hair abnormality (pili torti).
  • Cleft lip palate incisor and finger anomalies: A rare syndrome characterized by the association of a cleft lip and/or palate and anomalies involving the fingers and front teeth.
  • Cleft lip palate pituitary deficiency: A very rare disorder characterized by a cleft lip and palate as well as deficient pituitary gland activity which affects hormone levels. The clefts and the pituitary abnormality are considered to be midline defects.
  • Cleft lip with or without cleft palate: An oral clefting syndrome where a cleft lip is present with or without a cleft palate.
  • Cleft palate: This when there is a congenital fissure of the median line of the palate.
  • Cleft upper lip, median -- cutaneous polyps: A rare birth disorder characterized mainly by a cleft in the upper lip, central nervous system tumors and skin polyps.
  • Clefting -- ectropion -- conical teeth: A rare birth syndrome characterized by cleft lip and palate, cone-shaped teeth and everted lower eyelids.
  • Coloboma uveal with cleft lip palate and mental retardation: A very rare syndrome characterized by a cleft lip and palate, mental retardation and a gap or hole in the iris or uvea of the eye (iris or uveal coloboma).
  • Coloboma, cleft lip/palate and mental retardation syndrome: A very rare syndrome characterized by a cleft lip and palate, mental retardation and a gap or hole in the iris or uvea of the eye (iris or uveal coloboma).
  • Contractures -- ectodermal dysplasia -- cleft lip palate: A very rare syndrome characterized by impaired joint mobility at birth, skin problems, cleft lip or palate and growth and psychomotor retardation.
  • Cornelia de Lange syndrome 1: A very rare disorder involving delayed physical development and various malformations involving the head, face and limbs. Type 1 is more severe than type 2 though the range and severity of symptoms is variable.
  • Crane-Heise syndrome: A very rare fatal disorder characterized by numerous abnormalities.
  • Craniofacial dysostosis type 1: A rare genetic disorder characterized by premature joining of certain skull bones during development which has an impact on the shape of the head and face. Features include poor vision, hypoplasia of maxilla an impaired hearing.
  • Craniofrontonasal Syndrome: A congenital condition with multiple anomalies associated with mental retardation and skeletal disfigurement.
  • Craniofrontonasal dysplasia: A rare genetic disorder mainly found in females and characterized by premature closing of skull bones and craniofacial and limb abnormalities.
  • Craniosynostosis -- brachysyndactyly of hands and absence of toes: A rare condition characterized mainly by premature fusion of skull bones, limb defects and a cleft lip or palate.
  • Craniosynostosis cleft lip palate arthrogryposis: A rare condition characterized mainly by the association of premature fusion of skull bones (craniosynostosis), cleft lip and/or palate and arthrogryposis.
  • Craniosynostosis mental retardation clefting syndrome: A rare disorder characterized by premature fusion of the skull bones (craniosynostosis), mental retardation a cleft lip and/or palate.
  • Dandy-Walker -- facial hemangioma: A very rare syndrome characterized mainly by a brain malformation (Dandy-Walker) and a hemangioma on the face (mass of dilated blood vessels).
  • Decreased folate: Decrease in one of the B vitamins required for red blood cell production
  • Deformity symptoms: Various types of deformity
  • Del (2) (p22-p21): A rare chromosomal disorder characterized by various anomalies. The listed symptoms are those observed in one reported case. The manifestations linked to most genetic defects are often variable to some degree.
  • Del (2) (q12-q14): A rare chromosomal disorder characterized by various anomalies. The listed symptoms are those observed in two reported cases. The manifestations linked to most genetic defects are often variable to some degree.
  • Del (2) (q35-qter): A rare chromosomal disorder characterized by various anomalies. The listed symptoms are those observed in two reported cases. The manifestations linked to most genetic defects are often variable to some degree.
  • Del (3) (q12-q22): A rare chromosomal disorder characterized by various anomalies. The listed symptoms are those observed in one reported case. The manifestations linked to most genetic defects are often variable to some degree.
  • Del (3) (q28-qter): A rare chromosomal disorder characterized by various anomalies. The listed symptoms are those observed in one reported case. The manifestations linked to most genetic defects are often variable to some degree.
  • Del (4) (pter-p16) and dup (8) (pter-p21): A very rare chromosomal disorder where a portion of the short arm (pter-p16.3) of the genetic material on chromosome four is missing. The type and severity of symptoms can vary depending on the exact size and location of the deleted genetic material. The manifestations are similar to the main features of Wolf syndrome.
  • Del (4) (pter-p16.2): A rare syndrome characterized by the main features of Wolf syndrome which include profound mental retaradation and oral clefting.
  • Del (4) (pter-p16.2) and dup (2) (q37.1-qter): A rare syndrome characterized by the main features of Wolf syndrome which include profound mental retaradation and oral clefting. Patients tend to die soon after birth.
  • Del(1) (23-q25): A very rare chromosomal disorder where a portion of the long arm (23q-q25) of chromosome one is missing.
  • Del(1) (q25-q32): A very rare chromosomal disorder where a portion of the long arm (q25-q32) of chromosome one is missing. The range and severity of symptoms is variable.
  • Del(1) (q41-q43): A very rare chromosomal disorder where a portion of the long arm (q41-q43) of chromosome one is missing.
  • Deletion 10pter: A very rare syndrome caused by a chromosomal defect (10p terminal deletion) and can result in a variety of malformations that are similar to DiGeorge syndrome and velocardiofacial syndrome.
  • Deletion 2q: A rare chromosomal disorder where part of the long arm (q) of chromosome 2 is deleted resulting in various abnormalities which are determined by the size of the deleted portion.
  • Deletion 4p: A rare chromosomal disorder where part or all of the short arm (p) of chromosome 4 is deleted resulting in various abnormalities which are determined by the size of the deleted portion.
  • Deletion 6q: A rare chromosomal disorder where a part of the long arm (q) of chromosome 6 is deleted resulting in various abnormalities depending on the location and length of missing genetic material.
  • Deletion of the Short Arm of Chromosome 1: A condition characterized by deletion of the short arm of chromosome 1
  • Dincsoy-Salih-Patel syndrome: A very rare syndrome characterized mainly by a cleft lip and palate, brain abnormality, short limbs and genital abnormalities.
  • Dionisi-Vici-Sabetta-Gambarara syndrome: A very rare syndrome characterized mainly by brain abnormality, cataract and immunodeficiency.
  • Diprosopia: A very rare syndrome characterized by various facial anomalies, anencephaly and cleft lip and palate.
  • Dup (1) (q23-qter) and del (3)(pter-p25): A very rare chromosomal disorder where a portion of the long arm (q23-qter) of chromosome one and the short arm of chromosome 3 (pter- p25) is duplicated. In the reported case, the infant died soon after birth.
  • Dup (2) (pter-p21) and dup (21) (pter-q21): A rare chromosomal disorder characterized by various anomalies. The listed symptoms are those observed in one reported case. The manifestations linked to most genetic defects are often variable to some degree.
  • Dup (2) (q11.2-q13): A rare chromosomal disorder characterized by various anomalies. The listed symptoms are those observed in one reported case. The manifestations linked to most genetic defects are often variable to some degree.
  • Dup (3) (p26-p21.3) and del (3) (pter-p26): A rare chromosomal disorder characterized by various anomalies. The listed symptoms are those observed in one reported case. The manifestations linked to most genetic defects are often variable to some degree.
  • Dup (3) (pter-p14): A rare chromosomal disorder characterized by various anomalies. The listed symptoms are those observed in one reported case. The manifestations linked to most genetic defects are often variable to some degree.
  • Dup (3) (pter-p21) and del (18p): A rare chromosomal disorder characterized by various anomalies. The listed symptoms are those observed in two reported cases. The manifestations linked to most genetic defects are often variable to some degree.
  • Dup (3) (pter-p24) and del (4) (pter-p16): A rare chromosomal disorder characterized by various anomalies. The listed symptoms are those observed in six reported cases. The manifestations linked to most genetic defects are often variable to some degree.
  • Dup (3) (q24-q26): A rare chromosomal disorder characterized by various anomalies. The listed symptoms are those observed in one reported case. The manifestations linked to most genetic defects are often variable to some degree.
  • Dup(1) (p35-p31): A very rare chromosomal disorder where a portion of the short arm (p35-p31) of chromosome one is duplicated. The reported case resulted in death at 6 weeks of age.
  • Duplication 13: A rare and very severe chromosome disorder leading to mental retardation and physical defects. It is so severe that many babies die soon after birth. The type and severity of symptoms varies depending on the amount and exact location of the genetic material that is duplicated.
  • Dysraphism -- cleft lip palate -- limb reduction defects: A very rare syndrome characterized mainly by an abnormal opening in the lip and palate, forearm abnormalities, spinal cord defects and an abnormal abdominal opening allowing the abdominal contents to protrude.
  • Ectodermal dysplasia, Margarita type: A rare genetic disorder characterized by mental retardation, webbed digits, cleft lip, cleft palate, sparse hair, reduced sweating and teeth abnormalities. Progressive loss of scalp hair usually results in baldness by adulthood.
  • Ectodermal dysplasia, hypohidrotic, autosomal dominant: A very rare inherited disorder that affects the development of skin, hair, nails, teeth and sweat glands during the fetal stage.
  • Ectodermic dysplasia -- anhidrotic -- cleft lip:
  • Ectrodactyly -- Ectodermal Dysplasia -- Cleft Lip/Palate Syndrome, Type 1: EEC (Ectrodactyly, ectodermal dysplasia, cleft lip/palate) is a rare inherited condition characterized by split hand and foot deformities of variable severity, cleft lip or palate and teeth and hair anomalies. There are two main types of EEC which differ in the origin of the genetic defect. Type 1 is caused by a defect on chromosome 7q11. The severity and type of symptoms and deformities is highly variable.
  • Ectrodactyly -- Ectodermal Dysplasia -- Cleft Lip/Palate Syndrome, Type 3: EEC (Ectrodactyly, ectodermal dysplasia, cleft lip/palate) is a rare inherited condition characterized by split hand and foot deformities of variable severity, cleft lip or palate and teeth and hair anomalies. There are two main types of EEC which differ in the origin of the genetic defect. Type 3 is caused by a defect on chromosome 3q27. The severity and type of symptoms and deformities is highly variable.
  • Ectrodactyly-ectodermal dysplasia-cleft lip/cleft palate: A rare inherited condition characterized by abnormalities of the fingers, toes, hair, glands, eyes anr urinary tract.
  • Ellis -van creveld syndrome:
  • Ellis-van Creveld syndrome:
  • Endocrine-Cerebroosteodysplasia: A rare condition observed in six members from two families. The condition is severe with all affected individuals dying before, during or soon after birth. A number of the pregnancies were voluntarily terminated due to the detected malformations. Endocrine-Cerebroosteodysplasia primarily involves brain, skeletal and endocrine abnormalities.
  • Erythromycin -- Teratogenic Agent: There is evidence to indicate that exposure to Erythromycin (an antibiotic) during pregnancy may have a teratogenic effect on the fetus. A teratogen is a substance that can cause birth defects. The likelihood and severity of defects may be affected by the level of exposure and the stage of pregnancy that the exposure occurred at.
  • Eye defects -- arachnodactyly -- cardiopathy: A rare syndrome characterized mainly by eye defects, long, thin fingers and heart disease.
  • Face symptoms: Symptoms affecting the face
  • Facial clefting corpus callosum agenesis: A rare syndrome characterized by the association of facial clefts with a brain defect where the structure between the two halves of the brain (corpus callosum) fails to develop. Symptoms may vary somewhat depending on how much of the corpus callosum is missing and the extent of the facial clefting.
  • Fetal Hydantoin Syndrome: A rare disorder caused by fetal exposure to phenytoin (anticonvulsant drug) and resulting in various abnormalities.
  • Fetal alcohol syndrome: A condition which occurs in a new born fetus and is caused by the mother consuming excess alcohol during her pregnancy
  • Foramina parietalia permagna: A rare disorder involving abnormal bone development of the skull resulting in persistent wide fontanelles (cranium bifidum) as well as a scalp defect and other abnormalities.
  • Fraser Syndrome: A rare disorder characterized by the absence of one or both eyes as well as any of a number of other possible congenital abnormalities. Up to half of cases are stillborn.
  • Freire-Maia odontotrichomelic syndrome: A rare syndrome characterized by tooth, hair and limb abnormalities.
  • Freire-Maia syndrome: An extremely rare syndrome characterized by tooth, hair and limb abnormalities. The abnormalities can be quite severe in some cases. The parents may have been related in the reported cases.
  • Fronto-facio-nasal dysplasia: A very rare disorder involving skull and facial abnormalities.
  • Frontofacionasal dysplasia type Al gazali: A very rare disorder involving various serious facial abnormalities.
  • Frontonasal dysplasia: A very rare disorder involving head and face abnormalities primarily due to a groove down the midline of the face which may affect parts or all of the face.
  • Fryns Syndrome: A rare genetic disorder characterized by diaphragmatic abnormalities, coarse face and abnormal growth or development of ends of fingers and toes.
  • Gene-Wiedemann syndrome: An extremely rare birth disorder characterized by mental retardation and a variety of physical defects.
  • Genetic Disease: Any disease that is handed down to oneself through the chromosomes of ones parents
  • German syndrome: A rare disorder caused by fetal exposure to trimethadione (anticonvulsant drug) and resulting in various physical and developemental abnormalities.
  • Gollop syndrome: A rare syndrome characterized mainly by eye, ear, facial and nasal abnormalities.
  • Gonadal dysgenesis XY type associated anomalies: A very rare syndrome characterized mainly by a large range of variable physical abnormalities and gonad anoamlies.
  • Grob syndrome: A rare disorder characterized by a partial lack of hair, epicanthus, cleft lip and palate, mental deficiency, short fingers and various other anomalies.
  • Hardikar syndrome: A very rare disorder characterized by obstructive liver disease, cleft lip, cleft palate, eye and urogenital abnormalities.
  • Hay-Wells Syndrome: A rare genetic disorder characterized by ankyloblepharon, ectodermal dysplasia, and cleft lip and/or cleft palate.
  • Hay-Wells syndrome, recessive type: A rare recessively inherited genetic disorder characterized by ankyloblepharon, ectodermal dysplasia, and cleft lip and/or cleft palate. The recessive form of this condition is distinguished by the presence at birth of adhesions between the upper and lower jaws.
  • Head symptoms: Symptoms affecting the head or brain
  • Holoprosencephaly: A rare disorder where abnormalities of the fetal forebrain development lead to various birth defects.
  • Holoprosencephaly -- caudal dysgenesis: A very rare syndrome where the tailbone and the portion above the tailbone (coccyx and sacrum) fail to develop. The brain also fails to divide into two lobes resulting in a single-lobed brain
  • Holoprosencephaly -- ectrodactyly -- cleft lip/palate: A very rare syndrome characterized mainly by a cleft hand, lip and/or palate and the failure of the brain to separate into two lobes.
  • Holoprosencephaly deletion 2p: A very rare syndrome characterized mainly by the failure of the brain to separate into two lobes, facial deformities and various other anomalies.
  • Howard-Young syndrome: A very rare syndrome characterized mainly by a small head, facial cleft and an extra big toe.
  • Hunter-Carpenter-Macdonald syndrome: A very rare syndrome characterized by various abnormalities including small head, facial anomalies, mental retardation and hair, skin and nail anomalies. Fetal exposure to alcohol is believed to be a factor in the syndrome.
  • Hurst-Hallam-Hockey syndrome: A group of malformation described in a stillborn infant. Defects include leptomeningeal angiomatosis (abnormal blood vessels in sheath surrounding brain and spinal cord), heart disease, cleft lip and palate and brain abnormalities.
  • Hydrolethalus syndrome: A rare genetic disorder characterized by hydrocephalus, micrognathia and polydactyly.
  • Hypertelorism -- esophageal abnormalities -- hypospadias: A rare genetic disorder characterized by defects along the midline of the body. The type and severity of symptoms can vary considerably. There are two subtypes of the disorder: one is inherited in a X-linked manner and the other is inherited in an autosomal dominant manner. Females with the X-linked form of the condition tend to have few symptoms and often only have wide set eyes.
  • Hypertelorism with esophageal abnormality and hypospadias: A congenital disorder characterized by distinctive facial features, genital abnormalities, esophageal defect and difficulty swallowing. Males are more severely affected than females.
  • Hyperthermia induced defects: A rare disorder where hypothermia during pregnancy results in infant abnormalities involving growth, development and brain dysfunction.
  • Hypomelanosis of Ito: A rare genetic neurocutaneous disorder characterized by unusual patterns of depigmented skin and associated disorders such as seizures, psychomotor retardation and eye abnormalities.
  • Hypopituitarism -- micropenis -- cleft lip palate: A very rare syndrome characterized mainly by low pituitary hormone level, small penis and a cleft lip and palate.
  • Hypospadias -- hypertelorism: A congenital disorder characterized by distinctive facial features, genital abnormalities, esophageal defect and difficulty swallowing. Males are more severely affected than females.
  • Hypotelorism -- cleft palate -- hypospadias: A very rare syndrome characterized mainly by an abnormally placed urethral opening, cleft palate and close set eyes.
  • Incontinentia Pigmenti: A rare genetic skin pigmentation disorder characterized by eye, teeth, bone, nail and hair malformations as well as central nervous abnormalities and mental deficiency.
  • Iniencephaly: A rare type of neural tube defect where the head is positioned in a backward bent angle and the spine is malformed.
  • Isotretinoin embryopathy like syndrome: A very rare syndrome which causes the same abnormalities and deformities that occur in fetal exposure to maternal use of isotretinoin.
  • Joubert Syndrome: A rare neurological disorder where there is a defect in the part of the brain that controls coordination and balance.
  • Juberg-Hayward syndrome: A rare hereditary disorder characterized by a growth hormone deficiency as well as mouth and limb abnormalities.
  • Juvenile-onset dystonia: A rare form of progressive dystonia that starts early in life - first or second decade. Dystonia is prolonged involuntary muscle spasms or contractions. Various other physical abnormalities are also present and severe hearing loss usually occurs by the middle of the first decade. In the two reported cases, death occurred early in the third decade.
  • Kapur-Toriello syndrome: A rare disorder characterized by severe mental retardation, cleft lip, cleft palate, long columella (tissue that separates the nostrils) and eye, heart and intestinal abnormalities.
  • Klippel Feil deformity conductive deafness absent vagina: A rare developmental disorder occurring only in females and characterized by skeletal and genitourinary abnormalities and small stature.
  • Korula-Wilson-Salomonson syndrome: A very rare disorder characterized mainly by a cleft lip and palate and incomplete closure of the eyelids.
  • Kuster syndrome: A very rare congenital disorder characterized by a cleft lip, cleft palate, lip pits, and deformed limbs.
  • Lip pain: Pain or discomfort of the lips
  • Lip symptoms: Symptoms affecting one or both lips.
  • MURCS Association: A rare developmental disorder occurring only in females and characterized by skeletal and genitourinary abnormalities and small stature.
  • Mayer-Rokitansky-Kuster-Hauser, syndrome, type 2 (MRKH type 2): A rare developmental disorder occurring only in females and characterized by skeletal and genitourinary abnormalities and small stature.
  • Meckel syndrome, type 5: A very rare lethal syndrome characterized mainly by kidney and liver abnormalities, extra fingers and a gap in the back of the skull through which some brain matter protrudes. Type 5 is caused by a defect in the RPGRIP1L gene on chromosome 16q12.2.
  • Median cleft lip, corpus callosum, lipoma, and skin polyps: A very rare syndrome characterized mainly by a cleft lip, lipoma, skin polyps and abnormal brain development.
  • Median cleft, corpus callosum, lipoma, and cutaneous polyps:
  • Mende syndrome: A rare condition characterized by congenital deafness, mutism, partial albinism and a mongoloid face as well as other anomalies.
  • Meningeal angiomatosis -- cleft hypoplastic left heart: A very rare genetic disorder characterized by an underdeveloped left heart and abnormal brain development.
  • Mental retardation, Wolff type: A very rare syndrome characterized mainly by severe mental retardation and facial anomalies. The parents came from the same bloodline.
  • Mental retardation, X-linked, Siderius type: A rare inherited form of mental retardation involving a defect on chromosome Xp11.2.
  • Mephenytoin -- Teratogenic Agent: There is evidence to indicate that exposure to Mephenytoin during pregnancy may have a teratogenic effect on the fetus. A teratogen is a substance that can cause birth defects. The likelihood and severity of defects may be affected by the level of exposure and the stage of pregnancy that the exposure occurred at.
  • Microbrachycephaly -- ptosis -- cleft lip: A very rare syndrome characterized mainly by a small, short head, droopy eyelids and a cleft lip.
  • Microcephaly -- facial clefting -- preaxial polydactyly: A very rare condition characterized by the presence of an abnormally small head, facial clefts and extra digits.
  • Microcephaly -- microphthalmia -- ectrodactyly of lower limbs -- prognathism: A rare syndrome characterized by small eyes, small head, missing toes and a protrucing jaw.
  • Microcephaly immunodeficiency lymphoreticuloma: A very rare syndrome characterized mainly by a small head, reduced immunity and increased risk of cancer. There are a wide range of other abnormalities and symptoms that can occur.
  • Microcephaly, corpus callosum dysgenesis and cleft lip-palate: A rare disorder characterized by a small head, abnormal brain development and a cleft lip and palate.
  • Microphthalmia syndromic, type 8: A rare syndrome characterized by small eyes, small head, missing toes and protruding jaw.
  • Microsomia -- hemifacial -- radial defects: A very rare syndrome characterized mainly by a wide range of defects involving the face, ear, mouth, vertebrae and radial bones.
  • Midline cleft of lower lip: A very rare defect where there is a cleft in the middle of the lower lip.
  • Midline craniofacial anomalies and morning glory disc anomaly: A rare syndrome involving the association of midline skull and facial defects and morning glory disc anomaly - a rare birth defect of the optic papilla which is the part of the eye where the optic nerve emerges. The eye defect usually only affects one eye. The features are variable to some degree.
  • Midline field defects: Congenital problems that occur along the vertical axis of the body. Defects can involve the brain, spine, heart, genitals and midline of the head and face.
  • Mohr syndrome: A rare genetic disorder characterized by oral frenula, oral clefts, underdeveloped nose flaps and finger abnormalities.
  • Monosomy 18 Mosaic: An extremely rare chromosomal disorder where only some of the body's cells have one copy of chromosome 18 instead of the normal two. The severity and type of symptoms varies depending on how many and which body cells are affected.
  • Monosomy 18 mosaicism: An extremely rare chromosomal disorder where only some of the body's cells have one copy of chromosome 18 instead of the normal two. The severity and type of symptoms varies depending on how many and which body cells are affected.
  • Monosomy 1p36: A rare chromosomal disorder where deletion of a portion of chromosome 1 causes various abnormalities such as heart problems, mental retardation, developmental delay, facial dysmorphism and short stature. The range and severity of symptoms is variable with some cases being relatively mild.
  • Mouth symptoms: Symptoms of the mouth or oral area.
  • Mullerian Aplasia -- Renal Aplasia -- Cervicothoracic Somite Dysplasia: A rare developmental disorder occurring only in females and characterized by skeletal and genitourinary abnormalities and small stature.
  • Multiple congenital anomalies -- mental retardation -- growth failure and cleft lip/ palate: A very rare syndrome characterized mainly by mental retardation, growth failure, cleft lip, cleft palate and various other abnormalities.
  • Nijmegen Breakage Syndrome: A very rare syndrome characterized mainly by a small head, reduced immunity and increased risk of cancer. There are a wide range of other abnormalities and symptoms that can occur.
  • OFD syndrome type 8: A rare genetic disorder characterized by oral frenula, oral clefts, underdeveloped nose flaps and finger abnormalities.
  • OFD syndrome type Figuera: A rare genetic disorder characterized by oral frenula, oral clefts, underdeveloped nose flaps, finger abnormalities and absence of all or part of the fibula.
  • OFD syndrome type IX: A rare genetic disorder characterized by oral frenula, oral clefts, underdeveloped nose flaps and finger and retinal abnormalities.
  • Oculo-cerebro-acral, (Roberts-like)-ectrodactyly: A rare condition characterized by abnormalities of the eye, brain and extremeties as well as split hand and foot deformities.
  • Oculomaxillofacial dysostosis: A very rare syndrome characterized mainly by eye, jaw and facial abnormalities.
  • Oculopalatoskeletal syndrome: A very rare syndrome characterized mainly by eye, mouth palate and skeletal abnormalities.
  • Olanzapine -- Teratogenic Agent: There is evidence to indicate that exposure to Olanzapine during pregnancy may have a teratogenic effect on the fetus. A teratogen is a substance that can cause birth defects. The likelihood and severity of defects may be affected by the level of exposure and the stage of pregnancy that the exposure occurred at.
  • Opitz G Syndrome: A rare genetic disorder characterized by defects along the midline of the body. The type and severity of symptoms can vary considerably. There are two subtypes of the disorder: one is inherited in a X-linked manner and the other is inherited in an autosomal dominant manner. Females with the X-linked form of the condition tend to have few symptoms and often only have wide set eyes.
  • Opitz G/BBB Syndrome: A rare genetic disorder characterized by defects along the midline of the body. The type and severity of symptoms can vary considerably. There are two subtypes of the disorder: one is inherited in a X-linked manner and the other is inherited in an autosomal dominant manner. Females with the X-linked form of the condition tend to have few symptoms and often only have wide set eyes.
  • Opitz G/BBB Syndrome, Type II: A rare genetic disorder characterized by defects along the midline of the body. The type and severity of symptoms can vary considerably. There are two subtypes of the disorder: Type I inherited in a X-linked manner and type II is inherited in an autosomal dominant manner.
  • Opitz G/BBB Syndrome, X-linked: A rare genetic disorder characterized by defects along the midline of the body. The type and severity of symptoms can vary considerably. There are two subtypes of the disorder: type I is inherited in a X-linked manner and type II is inherited in an autosomal dominant manner. Females with type I tend to have few if any symptoms - often the only symptom is wide-set eyes.
  • Opitz G/BBB Syndrome, type I: A rare genetic disorder characterized by defects along the midline of the body. The type and severity of symptoms can vary considerably. There are two subtypes of the disorder: type I is inherited in a X-linked manner and type II is inherited in an autosomal dominant manner.
  • Opitz G/BBB syndrome, Autosomal dominant: A rare genetic disorder characterized by defects along the midline of the body. The type and severity of symptoms can vary considerably. There are two subtypes of the disorder: type I is inherited in a X-linked manner and type II is inherited in an autosomal dominant manner.
  • Opitz syndrome: A rare genetic disorder characterized by wide-set eyes, hypospadias and swallowing difficulties.
  • Opitz syndrome , X-linked: A congenital disorder characterized by distinctive facial features, genital abnormalities, esophageal defect and difficulty swallowing. Males are more severely affected than females.
  • Oral facial digital syndrome: A rare genetic disorder characterized by oral frenula, oral clefts, underdeveloped nose flaps and finger abnormalities.
  • Oral facial digital syndrome, type IV: A rare genetic disorder characterized by oral frenula, oral clefts, underdeveloped nose flaps, finger abnormalities, brain defects and short stature.
  • Oral-facial cleft: A birth defect involving an opening or cleft in the upper lip as well openings or clefts in the soft or hard palate (roof of the mouth)
  • Orofacial Cleft:
  • Orofacial Cleft 1: An orofacial cleft is a facial malformation present at birth. It can take the form of a cleft lip and/or a cleft palate. The degree of clefting affecting the lip and/or palate is variable. Researchers have discovered a number of genes linked to an increased susceptibility to being born with an orofacial cleft. Type 1 is linked to a genetic defect on chromosome 6p24.
  • Orofacial Cleft 10: An orofacial cleft is a facial malformation present at birth. It can take the form of a cleft lip and/or a cleft palate. The degree of clefting affecting the lip and/or palate is variable. Researchers have discovered a number of genes linked to an increased susceptibility to being born with an orofacial cleft. Type 10 is linked to a genetic defect on chromosome 2q32.2-q33.
  • Orofacial Cleft 11: An orofacial cleft is a facial malformation present at birth. It can take the form of a cleft lip and/or a cleft palate. The degree of clefting affecting the lip and/or palate is variable. Researchers have discovered a number of genes linked to an increased susceptibility to being born with an orofacial cleft. Type 11 is linked to a genetic defect on chromosome 14q22-q23.
  • Orofacial Cleft 12: An orofacial cleft is a facial malformation present at birth. It can take the form of a cleft lip and/or a cleft palate. The degree of clefting affecting the lip and/or palate is variable. Researchers have discovered a number of genes linked to an increased susceptibility to being born with an orofacial cleft. Type 12 is linked to a genetic defect on chromosome 8q34.3.
  • Orofacial Cleft 2: An orofacial cleft is a facial malformation present at birth. It can take the form of a cleft lip and/or a cleft palate. The degree of clefting affecting the lip and/or palate is variable. Researchers have discovered a number of genes linked to an increased susceptibility to being born with an orofacial cleft. Type 2 is linked to a genetic defect on chromosome 2p13.
  • Orofacial Cleft 3: An orofacial cleft is a facial malformation present at birth. It can take the form of a cleft lip and/or a cleft palate. The degree of clefting affecting the lip and/or palate is variable. Researchers have discovered a number of genes linked to an increased susceptibility to being born with an orofacial cleft. Type 3 is linked to a genetic defect on chromosome 19q13.
  • Orofacial Cleft 4: An orofacial cleft is a facial malformation present at birth. It can take the form of a cleft lip and/or a cleft palate. The degree of clefting affecting the lip and/or palate is variable. Researchers have discovered a number of genes linked to an increased susceptibility to being born with an orofacial cleft. Type 4 is linked to a genetic defect on chromosome 4q.
  • Orofacial Cleft 5: An orofacial cleft is a facial malformation present at birth. It can take the form of a cleft lip and/or a cleft palate. The degree of clefting affecting the lip and/or palate is variable. Researchers have discovered a number of genes linked to an increased susceptibility to being born with an orofacial cleft. Type 5 is linked to a genetic defect on chromosome 4p16.1.
  • Orofacial Cleft 6, Suseptibility to,: An orofacial cleft is a facial malformation present at birth. It can take the form of a cleft lip and/or a cleft palate. The degree of clefting affecting the lip and/or palate is variable. Researchers have discovered a number of genes linked to an increased susceptibility to being born with an orofacial cleft. Type 6 is linked to a genetic defect on chromosome 1q.
  • Orofacial Cleft 7: An orofacial cleft is a facial malformation present at birth. It can take the form of a cleft lip and/or a cleft palate. The degree of clefting affecting the lip and/or palate is variable. Researchers have discovered a number of genes linked to an increased susceptibility to being born with an orofacial cleft. Type 7 is linked to a genetic defect on chromosome 11q.
  • Orofacial Cleft 8: An orofacial cleft is a facial malformation present at birth. It can take the form of a cleft lip and/or a cleft palate. The degree of clefting affecting the lip and/or palate is variable. Researchers have discovered a number of genes linked to an increased susceptibility to being born with an orofacial cleft. Type 8 is linked to a genetic defect on chromosome 3q27.
  • Orofacial Cleft 9: An orofacial cleft is a facial malformation present at birth. It can take the form of a cleft lip and/or a cleft palate. The degree of clefting affecting the lip and/or palate is variable. Researchers have discovered a number of genes linked to an increased susceptibility to being born with an orofacial cleft. Type 9 is linked to a genetic defect on chromosome 13q33.1-q34.
  • Orofaciodigital syndrome Thurston type: A rare genetic disorder characterized by oral frenula, oral clefts, underdeveloped nose flaps and finger abnormalities.
  • Orofaciodigital syndrome type 10: A rare genetic disorder characterized by oral frenula, oral clefts, underdeveloped nose flaps, finger abnormalities and absence of all or part of the fibula.
  • Orofaciodigital syndrome, Shashi type: A rare genetic disorder involving oral, facial and digital abnormalities as well as the absence of the pituitary gland.
  • Orofaciodigital syndrome, type 3: A rare genetic disorder characterized by oral frenula, oral clefts, underdeveloped nose flaps and finger, teeth and eye abnormalities.
  • Palate symptoms: Symptoms affecting the palate
  • Partial Trisomy 3pter: A genetic disorder where a portion of the genetic material from the end of the short arm of chromosome 3 is duplicated so there are three copies instead of the normal two. The symptoms or severity may vary somewhat between patients depending on the size and location of the genetic material involved.
  • Phendimetrazine -- Teratogenic Agent: There is evidence to indicate that exposure to Phendimetrazine during pregnancy may have a teratogenic effect on the fetus. A teratogen is a substance that can cause birth defects. The likelihood and severity of defects may be affected by the level of exposure and the stage of pregnancy that the exposure occurred at.
  • Phenytoin -- Teratogenic Agent: There is evidence to indicate that exposure to Phenytoin during pregnancy may have a teratogenic effect on the fetus. A teratogen is a substance that can cause birth defects. The likelihood and severity of defects may be affected by the level of exposure and the stage of pregnancy that the exposure occurred at.
  • Pilotto syndrome: A very rare syndrome characterized mainly by congenital heart disease, cleft lip and palate, scoliosis, short stature and mental retardation.
  • Polydactyly cleft lip palate psychomotor retardation: A very rare syndrome described in a small inbred group of families and characterized by bifid toes, extra big fingers, cleft lip or palate and psychomotor retardation. There were various other symptoms that were variably present.
  • Polydactyly visceral anomalies cleft lip palate: A rare syndrome characterized mainly by the association of extra digits, cleft lip and/or palate and visceral anomalies. Various other abnormalities may also be present.
  • Popliteal pterygium syndrome: A rare genetic disorder characterized by cleft palate, pits in lower lip and popliteal webs.
  • Popliteal pterygium syndrome, lethal type: A rare lethal condition characterized by webbing of skin as well as various other physical and mental abnormalities.
  • Pseudotrisomy 13 syndrome: A very rare chromosomal disorder characterized mainly by abnormal forebrain development (holoprosencephaly), underdeveloped midface and extra fingers
  • Pterygium, Popliteal, lethal type: A rare lethal condition characterized by webbing of skin as well as various other physical and mental abnormalities.
  • Rapp-Hodgkin syndrome: A rare genetic multi-system disorder characterized by skin, teeth, hair and/or nail abnormalities, reduced ability to sweat and oral clefts.
  • Respiratory symptoms: Symptoms affecting the breathing systems.
  • Retention of tears -- ectrodactyly -- ectodermal dysplasia -- strange hair, skin and teeth: A rare syndrome characterized by a hand deformity and hair, skin and teeth abnormalities.
  • Richieri Costa Guion-Almeida syndrome: A very rare syndrome characterized mainly by mental retardation, short stature, cleft lip/palate and eye anomalies.
  • Roberts Pseudothalidomide Syndrome:
  • Roberts syndrome: A very rare genetic disorder involving a range of physical abnormalities.
  • Roberts-SC Phocomelia: A rare genetic disorder characterized by limb deformities, midfacial defects and severe growth deficiency.
  • Rubella congenital syndrome: The transplacental infection of a fetus with rubella
  • Samson-Viljoen syndrome: A very rare syndrome characterized by small ears, abnormal chest wall and facial, lip and palate clefts.
  • Schisis association: A medical term used to describe any condition involving two or more malformations of certain types. Malformations can include such things as oral clefts, neural tube defects, diaphragmatic hernias and omphaloceles.
  • Siderius type X-linked mental retardation syndrome: A rare inherited form of mental retardation involving a defect on chromosome Xp11.2. The symptoms are evident in males but females may be carriers.
  • Simvastatin -- Teratogenic Agent: There is evidence to indicate that exposure to Simvastatin during pregnancy may have a teratogenic effect on the fetus. A teratogen is a substance that can cause birth defects. The likelihood and severity of defects may be affected by the level of exposure and the stage of pregnancy that the exposure occurred at.
  • Single upper central incisor: A very rare syndrome characterized by various defects in the middle of the face.
  • Smith-Lemli-Opitz syndrome, type 2: A rare birth disorder where an enzyme deficiency (7-dehydrocholesterol reductase) prevents cholesterol being metabolized properly. The condition causes a variety of physical abnormalities. Type II is a more severe form of the condition.
  • Steinfeld syndrome: A very rare syndrome characterized by kidney abnormalities, single brain lobe and a heart defect.
  • Sugarman syndrome: A rare genetic disorder characterized by oral frenula, oral clefts, underdeveloped nose flaps and finger, teeth and eye abnormalities.
  • Tetra-Amelia, Autosomal Recessive: A recessively inherited malformation syndrome characterized by absence of all four limbs. Various other malformations were also present.
  • Tetraamelia with pulmonary hypoplasia: A very rare syndrome characterized mainly by the absence of arms and legs and abnormal lung development.
  • Tetramelic deficiencies -- Ectodermal dysplasia -- deformed ears -- other abnormalities: An extremely rare syndrome characterized by tooth, hair and limb abnormalities. The abnormalities can be quite severe in some cases. The parents may have been related in the reported cases.
  • Thomas Syndrome -- Potter Sequence with cleft lip/palate and cardiac anomalies: A rare condition characterized mainly by heart anomalies, a cleft lip or palate and Potter sequence which is a characteristic physical appearance observed in infants who experienced insufficient amniotic fluid in the womb.
  • Thomas syndrome: A very rare syndrome characterized mainly by heart malformations, kidney problems and cleft lip or palate.
  • Throat symptoms: Symptoms affecting the throat
  • Tibia absent -- polydactyly -- arachnoid cyst: A very rare syndrome characterized mainly by extra fingers, an absent shinbone and a brain cyst.
  • Tibial hemimelia -- cleft lip/palate: A very rare syndrome characterized by the association of a cleft lip or palate with a partially or completely absent shin bone.
  • Tobramycin -- Teratogenic Agent: There is evidence to indicate that exposure to Tobramycin during pregnancy may have a teratogenic effect on the fetus. A teratogen is a substance that can cause birth defects. The likelihood and severity of defects may be affected by the level of exposure and the stage of pregnancy that the exposure occurred at.
  • Tollner-Horst-Manzke syndrome: A very rare syndrome characterized by extra fingers, cleft lip, cleft palate and abdominal organ anomalies.
  • Triploid syndrome: A complete extra set of chromosomes.
  • Trisomy 13 mosaicism: A very rare chromosomal disorder where there is an extra copy of chromosome 13 in some of the body's cells. Some cases with this chromosomal abnormality have no clinical symptoms. The presence of abnormalities in some cases is dependent on which body cells contain the chromosomal defect. There appears to be a direct correlation between the number of cells in the body containing the chromosomal defect and severity of symptoms and survival.
  • Trisomy 3 mosaicism: A very rare chromosomal disorder where there is an extra copy of chromosome 3 in some of the body's cells. Some cases with this chromosomal abnormality have no clinical symptoms. The presence of abnormalities in some cases is dependent on which body cells contain the chromosomal defect.
  • Valproic acid antenatal infection: A condition which usually occurs in a fetus due to the mother taking valproic acid for epileptic seizures
  • Van der Woude syndrome: A syndrome which is characterised by multiple congenital abnormalities
  • Van der Woude syndrome 2: A syndrome which is characterised by multiple congenital abnormalities
  • Varadi Papp syndrome: A syndrome characterised by deformities of the oral-facial-digital areas
  • Verloove Vanhorick Brubakk syndrome: A syndrome that is characterised by the occurrence of cleft limbs and heart malformations.
  • W syndrome: A rare genetic disorder involving distinctive facial features, mental retardation, speech problems and limb deformities.
  • Waardenburg type pierpont: A rare disorder characterized mainly by a cleft palate and cleft lip as well as hearing problems and pigmentation anomalies. The combination of symptoms may vary somewhat with the cleft lip and palate being constant features.
  • Warfarin syndrome: Various physical and other abnormalities that can result from the use of the drug Warfarin during the first trimester of pregnancy.
  • Weaver Johnson syndrome: A syndrome that is characterised by craniosynostosis and cleft lip
  • Weaver Syndrome: A syndrome that is considered a variant of the Marshall-Smith syndrome
  • Whelan syndrome: A rare genetic disorder characterized by oral frenula, oral clefts, underdeveloped nose flaps, finger abnormalities and hydronephrosis.
  • Wolf-Hirschhorn Syndrome: A syndrome which is caused by a partial deletion of the short arm of chromosome 4.
  • Wolf-Hirschorn syndrome: A syndrome characterised by the partial deletion of the short arm of chromosome 4
  • Yim Ebbin syndrome: A congenital condition that results in several facial abnormalities
  • Zechi-Ceide Syndrome: A rare syndrome characterized mainly by a brain anomaly, unusual facial appearance and large feet. The three observed siblings were born to related parents and the range of anomalies was variable amongst them.
  • Zlotogora syndrome: A condition that is characterised by facial dysmorphism and psychiatric problems

Conditions listing medical symptoms: Cleft lip:

The following list of conditions have 'Cleft lip' or similar listed as a symptom in our database. This computer-generated list may be inaccurate or incomplete. Always seek prompt professional medical advice about the cause of any symptom.

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Conditions listing medical complications: Cleft lip:

The following list of medical conditions have 'Cleft lip' or similar listed as a medical complication in our database.

 

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