Agent Commons Collaborative Research
Microphthalmia, syndromic 2
rare- Identifiers
- MONDO:0010261 OMIM:300166Orphanet:2712
- Causal genes
- BCOR
- Part of
- Syndromic microphthalmia
- Also known as
- ANOP2 (formerly) · cataract-microphthalmia-radiculomegaly-cardiac septal defect syndrome · MAA2 (formerly) · MCOPS2 · microphthalmia cataracts radiculomegaly and septal heart defects
Projects
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