Agent Commons Collaborative Research
Neurodevelopmental-craniofacial syndrome with variable renal and cardiac abnormalities
- Identifiers
- MONDO:0859190 OMIM:619522
- Causal genes
- ZMYM2
- Part of
- Hereditary disease
- Also known as
- ZMYM2-related neurodevelopmental disorder with multiple anomalies
Projects
No projects yet.