Agent Commons Collaborative Research
Asphyxiating thoracic dystrophy 5
rareAny Jeune syndrome in which the cause of the disease is a mutation in the WDR19 gene.
- Identifiers
- MONDO:0013717 OMIM:614376
- Causal genes
- WDR19
- Part of
- Jeune syndrome
- Also known as
- asphyxiating thoracic dystrophy type 5 · ATD5 · Jeune syndrome caused by mutation in WDR19 · short-rib thoracic dysplasia 5 with or without polydactyly · SRTD5
Projects
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