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Symptoms » Tooth deformity » Glossary
 

Glossary for Tooth deformity

Medical terms related to Tooth deformity or mentioned in this section include:

  • AREDYLD: A rare condition characterized by abnormalities of the extremities, teeth, hair, nail and kidney as well as lipoatrophic diabetes.
  • Aarskog Syndrome: A rare genetic condition characterized by facial, hand, genital and growth abnormalities.
  • Acrofacial dysostosis, Weyers type: A rare disorder characterized by facial abnormalities and extra digits, nail abnormalities and short limbs.
  • Acutane embryopathy: A rare disorder caused by fetal exposure to retinoids and resulting in mental and physical birth defects.
  • Al Gazali-Khidr-Prem Chandran: A very rare syndrome characterized mainly by short stature, eye problems and an unusual cherubic facial appearance.
  • Al Gazali-Khidr-Prem Chandran syndrome:
  • Alves Castelo dos Santos syndrome: A rare syndrome characterized by hair, eye, skin and spinal abnormalities.
  • Amelo-cerebro-hypohidrotic syndrome: A rare syndrome involving degeneration of the central nervous system, seizures and abnormal tooth development.
  • Ampola syndrome: A rare genetic disease characterized primarily by mental retardation, facial anomalies, short stature, seizures and finger and toe abnormalities.
  • Ankylosis of teeth: A rare genetic disorder where the teeth fuse to the bone which can prevent them from erupting. Varying numbers of teeth may be affected.
  • Bosma-Henkin-Christiansen syndrome: A rare syndrome characterized mainly by a reduced sense of smell, an underdeveloped nose and hypogonadism.
  • Brachymetapody, anodontia, hypotrichosis, albinoidism: A rare syndrome characterized by short foot bones, total absence of teeth, reduced amount of hair and lack of skin pigmentation.
  • Breath symptoms: Breath-related symptoms including breath odor
  • Breathing symptoms: Symptoms affecting the breathing systems.
  • Cerebral Palsy: Any brain disorder causing movement disability
  • Cerebro-oculo-dento-auriculo-skeletal syndrome: A very rare syndrome characterized by abnormalities of the brain, eyes, teeth, ears and skeleton.
  • Charlie M syndrome: A rare birth disorder characterized by facial abnormalities and malformed or missing parts of the ends of the arms and legs.
  • Cherubism: An inherited condition marked by bone degradation of the jaws followed by development of fibrous tissue which causes the face to swell and hence have a cherubic appearance.
  • 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 8 recombinant syndrome: A rare recombinant chromosomal disorder involving chromosome 8 which results in various abnormalities.
  • Clefting -- ectropion -- conical teeth: A rare birth syndrome characterized by cleft lip and palate, cone-shaped teeth and everted lower eyelids.
  • Cleidocranial dysplasia: A rare genetic disorder characterized by collarbone defects, late ossification of cranial sutures and delayed tooth eruption.
  • Cone rod dystrophy -- amelogenesis imperfecta: A rare genetic disorder characterized by degeneration of parts of the eye that absorb light (cone rod dystrophy) as well as teeth abnormalities.
  • Congenital syphilis: Syphilis inherited from mother during pregnancy.
  • Deafness oligodontia syndrome: A rare disorder characterized by missing teeth and deafness.
  • Deafness onychodystrophy dominant form: A rare dominantly inherited disorder characterized by deafness from birth, deformed nails and
  • Deformity symptoms: Various types of deformity
  • Dental symptoms: Symptoms affecting teeth or mouth area.
  • Dentinogenesis Imperfecta Type III: A rare inherited dental disorder where the tops of primary and secondary teeth quickly erode leaving the inside of the tooth exposed.
  • Dentinogenesis imperfecta type Brandywine: A rare inherited dental disorder where the tops of primary and secondary teeth quickly erode leaving the inside of the tooth exposed.
  • Dentinogenesis imperfecta, type I: A rare inherited condition which occurs in people suffering from osteogenesis imperfecta (brittle bone disease) and is characterized by tooth structure abnormalities.
  • Dentinogenesis imperfecta, type II: A rare inherited dental disorder where the tops of primary and secondary teeth quickly erode leaving the inside of the tooth exposed.
  • Dermatoosteolysis, Kirghizian type: A rare condition characterized by a variety of abnormalities including missing teeth, recurring skin ulceration, eye problems and nail symptoms.
  • Developmental problems: Physical or mental development difficulty.
  • Down Syndrome: A chromosome syndrome causing physical effects and mental retardation.
  • Dup(1) (q25-q32): A very rare chromosomal disorder where a portion of the long arm (q25-q32) of chromosome one is duplicated. The type and severity of symptoms may vary.
  • Dysosteosclerosis: A rare inherited condition characterized by bone development abnormalities (excessive hardening of bone and flattened vertebrae), characteristic facial features. Excessive bone growth at the base of the skull can damage the optic nerves and affect vision.
  • Ectodermal dysplasia -- ectrodactyly -- macular dystrophy: A rare syndrome characterized mainly by skin, hair, nail and eye abnormalities as well as missing fingers.
  • Ectodermal dysplasia -- mental retardation -- central nervous system malformation: A rare syndrome characterized by severe mental retardation, hypothyroidism, abnormal brain development and hair, teeth and nail abnormalities.
  • Ectodermal dysplasia anhidrotic: A rare inherited condition involving skin, hair, teeth and nail abnormalities. The condition is characterized by the absence of sweat and sebaceous glands, underdeveloped hair and teeth, characteristic face and other physical deformities.
  • 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.
  • Ectodermal dysplasia, hypohidrotic, autosomal recessive: A rare genetic multisystem disorder characterized by hair, teeth, nail and skin abnormalities and absence of certain sweat glands.
  • Ectodermal dysplasia, hypohidrotic, with immune deficiency: A rare genetic disorder characterized inability to sweat, immune system problems and hair and teeth abnormalities.
  • Edentulism: Without teeth
  • Ehlers danlos syndrome: An inherited disorder of the connective tissue causing it to become weak and fragile. Connective tissue is found in skin, muscles, tendons and ligaments and hence all of these may be affected by weakness
  • Ehlers-Danlos syndrome: An inherited disorder of the connective tissue causing it to become weak and fragile. Connective tissue is found in skin, muscles, tendons and ligaments and hence all of these may be affected by weakness
  • Ellis -van creveld syndrome:
  • Ellis-van Creveld syndrome:
  • Epidermolysis bullosa, late-onset, localized junctional, with mental retardation: A rare genetic disorder characterized by mental retardation, hair and nail disorders, absence of teeth and areas fragile skin that blisters easily.
  • Face symptoms: Symptoms affecting the face
  • Gene-Wiedemann syndrome: An extremely rare birth disorder characterized by mental retardation and a variety of physical defects.
  • 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
  • Hooft disease: A rare disorder characterized by mental and physical retardation, red rash and low blood lipid level.
  • Hypermethioninemia due to S-adenosylhomocysteine hydrolase deficiency: A rare disorder involving an enzyme deficiency which results in increased methionine levels in the blood. The condition manifests as psychomotor delay and severe muscle disease.
  • Hypoparathyroidism X-linked: Low parathyroid levels inherited in a X-linked manner and hence only males are symptomatic and females are asymptomatic carriers.
  • Hypothyroidism: The decreased activity of the thyroid gland
  • 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.
  • Injury: Any damage inflicted in the body
  • Johanson-Blizzard Syndrome: A rare genetic disorder involving a range of abnormalities including a characteristic beak-like small nose, hypothyroidism and deafness.
  • Jorgenson syndrome: A rare inherited syndrome characterized by hair, teeth and skin abnormalities. The hair may be normal at birth but becomes sparse by the second decade.
  • Koussef nichols syndrome: A very rare syndrome characterized mainly by muscle problems, a high body temperature and various other physical abnormalities.
  • Kousseff-Nichols syndrome: A very rare syndrome characterized mainly by muscle problems, a high body temperature and various other physical abnormalities.
  • Lobstein disease: A group of rare inherited diseases that involves fragile bones. There are many different types based on the severity and extent of symptoms. Some types are severe enough to cause stillbirth or infant death whereas other types may cause few if any problematic symptoms.
  • Lockwood-Feingold syndrome: A rare genetic disorder characterized mainly by arthritis, skeletal abnormalities and a lack of subcutaneous fat.
  • Marinesco-Sjogren I: A rare condition characterized by cerebellar ataxia, speaking difficulty, mental retardation, short stature and tooth, hair and nail abnormalities.
  • Meinecke syndrome: A very rare syndrome characterized mainly by mental retardation and short broad thumbs.
  • Mental retardation -- macrocephaly -- coarse facies -- hypotonia: A very rare syndrome characterized mainly by mental retardation, large head, coarse face and reduced muscle tone.
  • Mental retardation unusual facies ampola type: A rare genetic disease characterized primarily by mental retardation, facial anomalies, short stature, seizures and finger and toe abnormalities.
  • Mental retardation, Buenos Aires type: A very rare syndrome characterized mainly by mental retardation, physical retardation, unusual facial appearance and heart and kidney defects.
  • Mouth symptoms: Symptoms of the mouth or oral area.
  • Nance-Horan Syndrome: An inherited congenital condition characterized mainly by cataracts and peg-shaped and extra teeth
  • Nutritional deficiency: Any deficiency of the nutrients that are required to sustain human life
  • OFD syndrome type 8: A rare genetic disorder characterized by oral frenula, oral clefts, underdeveloped nose flaps and finger abnormalities.
  • OLEDAID: A rare syndrome characterized mainly by a weak immuned system, bone problems, lymphoedema and hair, teeth and nail abnormalities. Death usually occurs during the first few years of life due to overwhelming infections.
  • Oculodental syndrome: A familial disorder characterized by corneal dystrophy, enlarged gums and missing teeth
  • Oculodentoosseous dysplasia recessive: A very rare recessively inherited syndrome characterized mainly by eye, tooth and finger abnormalities. The eye abnormalities tend to be more severe than in the dominant form of the disorder.
  • Odonto onycho dysplasia with alopecia: A very rare syndrome characterized mainly by tooth, nail and hair abnormalities.
  • Odontoonychodermal dysplasia: A very rare syndrome characterized mainly by tooth, nail and skin abnormalities.
  • Oligodontia, keratitis, skin ulceration and arthroosteolysis: A rare condition characterized by a variety of abnormalities including missing teeth, recurring skin ulceration, eye problems and nail symptoms.
  • Osteogenesis imperfecta type II: A rare lethal form of the genetic connective tissue disorder characterized by fragile bones, blue sclerae and facial and tooth abnormalities.
  • Osteogenesis imperfecta, type 2: A rare lethal form of the genetic connective tissue disorder characterized by fragile bones, blue sclerae and facial and tooth abnormalities.
  • Osteogenesis imperfecta, type 2A: A rare lethal form of a genetic connective tissue disorder characterized by fragile bones, blue sclerae and facial and tooth abnormalities. Type IIA has a different origin of the genetic mutation but the clinical features are similar. Type IIA involves a defect on the COL1A2 gene. The main difference is that type IIA tends to involve a large head and dark blue eyes.
  • Osteogenesis imperfecta, type IIB: A rare, recessively inherited, lethal form of a genetic connective tissue disorder characterized by fragile bones, blue sclerae and facial and tooth abnormalities. Type IIB has a different origin of the genetic mutation but the clinical features are similar. Type IIB involves a defect on the CRTAP gene on chromosome 3p22. The main difference is that type IIA tends to involve a small head and white or light blue eyes.
  • Osteosclerosis, abnormalities of nervous system and meninges: A very rare syndrome characterized mainly by increased bone density and nervous system abnormalities.
  • Pallister-Ulnar mammary syndrome: A rare genetic condition characterized by extra or missing digits, breast and dental abnormalities.
  • Pregnancy symptoms: Symptoms related to pregnancy.
  • Progeria: A rare fatal genetic disorder characterized by extremely premature aging.
  • Rabson-Mendenhall syndrome: A very rare genetic disorder involving severe insulin resistance which is where the body fails to be able to use insulin which is needed to control blood sugar levels.
  • Radioulnar synostosis mental retardation hypotonia: A very rare syndrome involving mental retardation, reduced muscle tone and fusion of the forearm bones.
  • 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.
  • Retinoids embryopathy: Fetal exposure to retinoids has the potential to cause mental and physical birth defects, particularly craniofacial, heart and ear malformations. It is advised that women planning a pregnancy should avoid taking retinoids for two years before the pregnancy.
  • Rickets: A condition that affects the bones due to vitamin D deficiency
  • Robinow Sorauf syndrome: A rare disorder characterized by facial and dental abnormalities as well as a partial or complete duplication of the end bone of the big toe.
  • Robinson-Miller-Bensimon syndrome: A very rare syndrome characterized by deafness, malformed nails and other abnormalities.
  • SCARF syndrome: A rare syndrome characterized mainly by skeletal abnormalities, loose skin, premature fusion of skull bones, ambiguous genitalia, psychomotor retardation and facial abnormalities.
  • Sclerosing bone dysplasia -- mental retardation: A rare disorder characterized by abnormal hardening (sclerosis) of the bone and mental retardation.
  • Short stature -- valvular heart disease: A very rare syndrome characterized mainly by short stature and heart valve disease.
  • Singh-Chhaparwal-Dhanda syndrome: A very rare syndrome characterized mainly by short stature, mental retardation, eye defects and a missing kneecap.
  • Skeletal symptoms: Symptoms affecting the skeletal system such as the bones.
  • Stoll-Alembik-Finck syndrome: A very rare syndrome characterized mainly by muscle, skin, sweating, tooth and facial abnormalities.
  • Stoll-Levy-Fancfort syndrome: A rare syndrome characterized mainly by deafness, missing fingers, abnormal heart rhythm and missing bones in limbs.
  • Thiele syndrome: A very rare syndrome characterized mainly by mental retardation, unusual facial appearance and a small head.
  • Throat symptoms: Symptoms affecting the throat
  • Thumb deformity, alopecia, pigmentation anomaly: A very rare syndrome characterized mainly by a deformed thumb, lack of hair and abnormal pigmentation.
  • Tooth pain: Toothache due to infectious or non-infectious etiology.
  • Tricho odonto onycho dermal syndrome: A very rare syndrome characterized by hair, tooth, nail and skin abnormalities.
  • Trueb-Burg-Bottani syndrome: A very rare genetic syndrome characterized by hair, teeth and nail abnormalities as well as webbed fingers.
  • Zadik Barak Levin syndrome: A condition that affects the endocrine system as well as some facial characteristics

Conditions listing medical symptoms: Tooth deformity:

The following list of conditions have 'Tooth deformity' 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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