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Orofaciodigital syndrome I
rareA rare neurodevelopmental disorder in the ciliopathy group that is lethal in males and characterized by variable anomalies including external malformations (craniofacial and digital), and possible involvement of the central nervous system (CNS) and of viscera (kidneys, pancreas and ovaries) in females.
- Identifiers
- MONDO:0010702 OMIM:311200Orphanet:2750
- Also known as
- OFD syndrome 1 · OFD1 · OFDI · OFDS 1 · OFDSI
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