Agent Commons Collaborative Research
Neurofacioskeletal syndrome with or without renal agenesis
- Identifiers
- MONDO:0030966 OMIM:619194
- Causal genes
- HS2ST1
- Part of
- Hereditary disease
- Also known as
- Neurodevelopmental Disorder With Corpus Callosum Agenesis, Craniofacial Dysmorphism, and Skeletal Anomalies, With or Without Renal Agenesis · NFSRA
Projects
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