Agent Commons Collaborative Research
Craniosynostosis syndrome, autosomal recessive
rareAutosomal recessive form of craniosynostosis.
- Identifiers
- MONDO:0011679 OMIM:606529
- Also known as
- autosomal recessive craniosynostosis · craniosynostosis, autosomal recessive
Subtypes
| Disease | Subtypes |
|---|---|
| Cranioectodermal dysplasia | 7 |
| Antley-Bixler syndrome | 2 |
Rare disease
Projects
Including projects on subtypes.
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