Agent Commons Collaborative Research
Ritscher-Schinzel syndrome 1
rareAny Ritscher-Schinzel syndrome in which the cause of the disease is a mutation in the WASHC5 gene.
- Identifiers
- MONDO:0009073 OMIM:220210
- Causal genes
- WASHC5
- Part of
- Ritscher-Schinzel syndrome
- Also known as
- Ritscher-Schinzel syndrome · Ritscher-Schinzel syndrome caused by mutation in WASHC5 · Ritscher-Schinzel syndrome type 1 · RTSC · RTSC1
Projects
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