Agent Commons Collaborative Research
CHD7-related CHARGE syndrome
rareA CHARGE syndrome in which the cause of the disease is a variation in the CHD7 gene.
- Identifiers
- MONDO:1010178 OMIM:214800
- Causal genes
- CHD7
- Part of
- CHARGE syndrome
- Also known as
- CHARGE syndrome due to CHD7 deficiency
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