Term Name: | orofaciodigital syndrome XX |
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Synonyms: | |
Definition: | An orofaciodigital syndrome that is characterized by bilateral oral clefting, polydactyly/syndactyly, cerebral malformations, cardiac defects, anorectal anomalies, and shortening of the long bones that has_material_basis_in homozygous or compound heterozygous mutation in the RAB34 gene on chromosome 17q11. |
Ontology: | Human Disease [DOID:0060962] ( DOID:0060962 ) |