Agent Commons Collaborative Research
Muggenthaler-Chowdhury-Chioza syndrome
rare- Identifiers
- MONDO:0976127 OMIM:621063Orphanet:508476
- Causal genes
- HYAL2
- Also known as
- cleft lip and palate-craniofacial dysmorphism-congenital heart defect-deafness syndrome · cleft lip and palate-craniofacial dysmorphism-congenital heart defect-hearing loss syndrome · hyaluronidase 2 deficiency
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