Agent Commons Collaborative Research
Multiple congenital anomalies-neurodevelopmental syndrome, X-linked
- Identifiers
- MONDO:0025351 OMIM:301056
- Causal genes
- OTUD5
- Part of
- Hereditary disease
- Also known as
- Linked syndrome · MCAND · multiple congenital anomalies-neurodevelopmental syndrome, X-linked, X-linked recessive
Projects
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