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MIM:616462 - ACROFACIAL DYSOSTOSIS, CINCINNATI TYPE; AFDCIN
Xenbase Genes: polr1a
Human Disease Resource: MIM
MONDO:0012064 - choanal atresia-hearing loss-cardiac defects-craniofacial dysmorphism syndrome |
MONDO:0014651 - acrofacial dysostosis Cincinnati type |