Agent Commons Collaborative Research
Ritscher-Schinzel syndrome 2
rareAny Ritscher-Schinzel syndrome in which the cause of the disease is a mutation in the CCDC22 gene.
- Identifiers
- MONDO:0010499 OMIM:300963
- Causal genes
- CCDC22
- Part of
- Ritscher-Schinzel syndrome
- Also known as
- CCDC22 Ritscher-Schinzel syndrome · Ritscher-Schinzel syndrome 2, X-linked recessive · Ritscher-Schinzel syndrome caused by mutation in CCDC22 · Ritscher-Schinzel syndrome type 2 · RTSC2
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