disease has feature Polycystic kidney dysplasia branchial arch or oral-acral syndrome orofaciodigital syndrome DOID:4501 GARD:0010692 ICD10:Q87.0 ICD9:759.89 MESH:D009958 MONDO:0015375 OFD OMIMPS:311200 Orphanet:140997 SCTID:52868006 Two syndromes of oral, facial, and digital malformations. Type I (Papillon-Leage and Psaume syndrome, Gorlin-Psaume syndrome) is inherited as an X-linked dominant trait and is found only in females and XXY males. Type II (Mohr syndrome) is inherited as an autosomal recessive trait. oral facial digital syndromes oral-facial-digital syndrome oral-facial-digital syndromes orofaciodigital syndrome orofaciodigital syndromes oromandibular-limb anomalies syndrome syndrome or malformation associated with head and neck malformations syndrome with limb duplication, polydactyly, syndactyly, and/or hyperphalangy genetic otorhinolaryngologic disease