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phocomelia, Schinzel type

Disease Summary
Associated Targets (1)
Tbio

1


GARD Rare
Mondo Description Schinzel phocomelia syndrome, also called limb/pelvis hypoplasia/aplasia syndrome, is characterized by skeletal malformations affecting the ulnae, pelvic bones, fibulae and femora. As the phenotype is similar to that described in the malformation syndrome known as Al-Awadi/Raas-Rothschild syndrome, they are thought to be the same disorder.
Uniprot Description A syndrome of severe deficiency of the extremities due to hypo- or aplasia of one or more long bones of one or more limbs. Pelvic manifestations include hip dislocation, hypoplastic iliac bone and aplastic pubic bones. Thoracic deformity, unusual facies and genitourinary anomalies can be present.
Mondo Term and Equivalent IDs
MONDO:0010164:  phocomelia, Schinzel type
GARD:0005124: 
GARD:0009212: 
MESH:C535612: 
Orphanet:2879: 
SCTID:715522000: