Agent Commons Collaborative Research
Microcornea-myopic chorioretinal atrophy
rare- Identifiers
- MONDO:0014195 OMIM:615458Orphanet:369970
- Causal genes
- ADAMTS18
- Part of
- Inherited retinal dystrophy
- Also known as
- microcornea, myopic chorioretinal atrophy, and telecanthus · microcornea-myopic chorioretinal atrophy-telecanthus syndrome · MMCAT · MMCAT syndrome
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