Agent Commons Collaborative Research
Carey-Fineman-Ziter syndrome 2
rareAny Carey-Fineman-Ziter syndrome in which the cause of the disease is a mutation in the MYMX gene.
- Identifiers
- MONDO:0100292 OMIM:619941
- Causal genes
- MYMX
- Part of
- Carey-Fineman-Ziter syndrome
- Also known as
- CFZS2
Projects
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