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Symptoms » Abnormal rib number » Glossary

Glossary for Abnormal rib number

Medical terms related to Abnormal rib number or mentioned in this section include:

  • 3C syndrome: A rare disorder characterized by cardiac malformations, cerebellar hypoplasia and cranial dysmorphism which gives the disease it's name.
  • Abnormal pain: The abnormal presence of pain that one may feel
  • Acrofacial dysostosis Rodriguez type: One of a group of disorders characterized by defective limb and facial development. The Rodriguez type is very rare and primarily involves severe limb and organ malformations.
  • Agnathia-holoprosencephaly-situs inversus: A very rare disorder characterized by a small or absent jaw, developmental brain defect and internal organs situated on the wrong side of the body (situs inversus). The severity and range of symptoms is variable.
  • Aural atresia -- multiple congenital anomalies -- mental retardation: A rare syndrome characterized by a number of malformations as well as mental retardation.
  • Bone symptoms: Symptoms affecting the body's bones
  • Campomelia Cumming type: A rare syndrome characterized by limb and multiple abdominal organ abnormalities. The disorder results in death before birth or soon after.
  • Campomelic dysplasia: A rare genetic disorder characterized by bowed tibia, underdeveloped shoulder blades and a flat face.
  • Chest symptoms: Symptoms affecting the chest region.
  • Chromosome 1, deletion q21 q25: A rare chromosomal disorder where deletion of a portion of chromosome 1 causes various abnormalities such as retarded fetal growth, osteoporosis, facial anomalies and hearing loss.
  • Chromosome 1, monosomy 1q4: A rare chromosomal disorder where deletion of a portion of chromosome 1 causes various abnormalities such as facial dysmorphism, retarded fetal growth, seizures, mental retardation, testicular problems and kidney defects.
  • Cleidocranial dysplasia: A rare genetic disorder characterized by collarbone defects, late ossification of cranial sutures and delayed tooth eruption.
  • Developmental problems: Physical or mental development difficulty.
  • Game-Friedman-Paradice syndrome: A rare condition characterized by retarded growth, hydrocephaly, underdeveloped lungs and various other anomalies. The condition was observed in four offspring from one family.
  • Growth symptoms: Symptoms related to poor or excessive growth.
  • Head symptoms: Symptoms affecting the head or brain
  • Herrmann-Opitz craniosynostosi: A very rare syndrome characterized mainly by mental retardation, skeletal abnormalities and an unusual facial appearance.
  • Infant symptoms: Symptoms affecting babies and infants.
  • Lethal chondrodysplasia, Moerman type: A very rare lethal syndrome characterized mainly by abnormal bone development.
  • Limb symptoms: Symptoms affecting the limbs
  • Manouvrier syndrome: A very rare syndrome characterized mainly by the failure of the lungs to develop fully, heart defects and thumb abnormalities.
  • Melhem-Fahl syndrome: A very rare syndrome characterized mainly by an abnormal number of ribs and vertebrae.
  • Microcephalic primordial dwarfism, Toriello type: A very rare syndrome characterized mainly by dwarfism, mental retardation and other anomalies.
  • Microlissencephaly -- micromelia: A rare syndrome characterized mainly by short arms, a brain defect called microlissencephaly, small head and early death.
  • Poor growth: Poor body growth or delayed physical development.
  • Proximal spinal muscular atrophy: A rare group of muscle disorders which mainly affects the muscles closest to the trunk of the body. Muscles become progressively weak and wasted due to damage to motor neurons in the spinal cord and brainstem.
  • Rib disorder:
  • Rib pain: Pain occurring on or around the ribs.
  • Rib symptoms: Symptoms affecting the ribs
  • Rommen-Mueller-Sybert syndrome: A very rare syndrome characterized mainly by heart defects, short stature and craniofacial anomalies.
  • Skeletal symptoms: Symptoms affecting the skeletal system such as the bones.
  • Spondylocostal dysostosis, autosomal recessive: A rare, recessively inherited syndrome characterized mainly by rib and spine abnormalities. The recessive form is more severe than the dominantly inherited form.
  • Tetraamelia -- multiple malformations: A very rare syndrome characterized mainly by a lack of arm and leg bones (hands and feet are still present) as well as other malformations.
  • Tsukuhara syndrome: A very rare syndrome characterized mainly by a curved spine, premature fusion of skull bones and a small head.

Conditions listing medical symptoms: Abnormal rib number:

The following list of conditions have 'Abnormal rib number' 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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