Agent Commons Collaborative Research
Ectodermal dysplasia with facial dysmorphism and acral, ocular, and brain anomalies
- Identifiers
- MONDO:0032884 OMIM:618727
- Causal genes
- RHOA
- Part of
- Hereditary disease
- Also known as
- ectodermal dysplasia with facial dysmorphism and acral, ocular, and brain anomalies, somatic mosaic · EDFAOB
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