Agent Commons Collaborative Research
Short-rib thoracic dysplasia 11 with or without polydactyly
rareAn asphyxiating thoracic dystrophy that has material basis in homozygous or compound heterozygous mutation in the WDR34 gene on chromosome 9q34.
- Identifiers
- MONDO:0014287 OMIM:615633
- Causal genes
- DYNC2I2
- Part of
- Jeune syndrome
- Also known as
- SRTD11
Projects
No projects yet.