deafness-craniofacial syndrome https://rarediseases.info.nih.gov/diseases/1686/deafness-craniofacial-syndrome https://www.malacards.org/card/deafness_craniofacial_syndrome_2 SCTID:716245003 GARD:0001686 MESH:C565118 MONDO:0007428 deafness craniofacial syndrome Deafness-craniofacial syndrome is characterized by the association of congenital hearing loss and facial dysmorphism (facial asymmetry, a broad nasal root and small nasal alae). It has been described in two members (father and daughter) of one Jewish family. Temporal alopecia was also noted. Transmission appeared to be autosomal dominant. OMIM:125230 UMLS:C1852278 Orphanet:3241 deafness-craniofacial syndrome MEDGEN:342201 multiple congenital anomalies/dysmorphic syndrome without intellectual disability