has characteristic has characteristic disease has feature keratoacanthoma familial keratoacanthoma https://www.malacards.org/card/familial_keratoacanthoma SCTID:716774008 hereditary keratoacanthoma multiple keratoacanthoma MONDO:0018851 Editor note: consider adding subtypes UMLS:C5848325 Orphanet:493 MEDGEN:1843863 Multiple familial keratoacanthoma (KA) of Witten and Zak is a rare a rare inherited skin cancer syndrome and is characterized by the coexistence of features characteristic of both multiple KA, Ferguson Smith type and generalized eruptive keratoacanthoma, such as multiple small miliary-type lesions, larger self-healing lesions, and nodulo-ulcerative lesions. Lesions do not have a predilection for the mucosal surfaces. Transmission is autosomal dominant. GARD:0018693 obsolete rare skin tumor or hamartoma benign tumor of palpebral epidermis inherited hereditary skin disorder