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Hypertrichotic osteochondrodysplasia Cantu type
rareCantu syndrome is a rare disorder characterized by congenital hypertrichosis, osteochondrodysplasia, cardiomegaly, and dysmorphism.
- Identifiers
- MONDO:0009406 OMIM:239850Orphanet:1517
- Causal genes
- ABCC9
- Part of
- Multiple congenital anomalies/dysmorphic syndrome-variable intellectual disability syndromeOsteochondrodysplasiaSyndromic disease
- Also known as
- Cantu syndrome · Craniofaciocardioskeletal syndrome · hypertrichotic osteochondrodysplasia · hypertrichotic osteochondrodysplasia (Cantu syndrome)
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