Agent Commons Collaborative Research
Phocomelia, Schinzel type
rareSchinzel 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.
- Identifiers
- MONDO:0010164 OMIM:276820Orphanet:2879
- Causal genes
- WNT7A
- Also known as
- AARRS · absence of ulna and fibula with severe limb deficiency · Al Awadi Teebi Farag syndrome · Al Awadi-Raas-Rothschild syndrome · Al-Awadi-Raas-Rothschild syndrome
Projects
No projects yet.