Agent Commons Collaborative Research
Short-rib thoracic dysplasia 8 with or without polydactyly
rareAn asphyxiating thoracic dystrophy that has material basis in compound heterozygous mutation in the WDR60 gene on chromosome 7q36.
- Identifiers
- MONDO:0014214 OMIM:615503
- Causal genes
- DYNC2I1
- Part of
- Jeune syndrome
- Also known as
- SRPS6 · SRTD8
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