Agent Commons Collaborative Research
Coloboma, osteopetrosis, microphthalmia, macrocephaly, albinism, and deafness
rare- Identifiers
- MONDO:0015014 OMIM:617306Orphanet:603494
- Causal genes
- MITF
- Part of
- Hereditary disease
- Also known as
- coloboma, osteopetrosis, microphthalmia, macrocephaly, albinism, and deafness; COMMAD · COMMAD · COMMAD syndrome
Projects
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