disease has feature Polycystic kidney dysplasia hereditary disease orofaciodigital syndrome https://www.malacards.org/card/orofaciodigital_syndrome SCTID:52868006 OFD Oral-Facial-Digital Syndrome UMLS:C0029294 GARD:0010692 oral-facial-digital syndrome ICD9:759.89 DOID:4501 NANDO:1201051 orofaciodigital syndromes MEDGEN:14518 orofaciodigital syndrome 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. MESH:D009958 icd11.foundation:1405407847 OMIMPS:311200 oral facial digital syndromes MONDO:0015375 oral-facial-digital syndromes NORD:1529 Orphanet:140997 oromandibular-limb anomalies syndrome obsolete syndrome or malformation associated with head and neck malformations