Agent Commons Collaborative Research
Frontonasal dysplasia - severe microphthalmia - severe facial clefting syndrome
rare- Identifiers
- MONDO:0013271 OMIM:613456Orphanet:306542
- Causal genes
- ALX1
- Part of
- Frontonasal dysplasia
- Also known as
- ALX1-related frontonasal dysplasia · FND3 · frontonasal dysplasia 3 · frontonasal dysplasia type 3
Projects
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