Agent Commons Collaborative Research
Aplasia cutis-enamel dysplasia syndrome
rare- Identifiers
- MONDO:0968978 OMIM:620789Orphanet:697356
- Causal genes
- FOSL2
- Also known as
- Congenital scalp aplasia cutis-enamel hypoplasia-developmental delay-intellectual disability syndrome · FOSL2-related neurodevelopmental disorder
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