A genetic skin disease characterized by hypoplasia of the dermis, herniations of fat, and hand anomalies. It is found exclusively in females and transmitted as an X-linked dominant trait.
Synonyms: Focal Dermal Hypoplasia, Dermal Hypoplasia, Focal, Hypoplasias, Focal Dermal, Goltz-Gorlin Syndrome, Syndrome, Goltz Gorlin, Goltz's Syndrome, Gorlin Syndrome, Goltz, Syndrome, Goltz's, Goltz Gorlin Syndrome, Goltz Syndrome, Syndrome, Goltz-Gorlin, Syndrome, Goltz, Goltzs Syndrome, Focal Dermal Hypoplasias, Hypoplasia, Focal Dermal, Dermal Hypoplasias, Focal
Instance information
91(85); was see under ECTODERMAL DYSPLASIA 1987-90, was see under ECTODERMAL DEFECT, CONGENITAL 1985-86; GOLTZ-GORLIN SYNDROME was see FOCAL DERMAL HYPOPLASIA 1985-92 ,91; was see under ECTODERMAL DYSPLASIA 1987-90, was see under ECTODERMAL DEFECT, CONGENITAL 1985-86; GOLTZ-GORLIN SYNDROME was see FOCAL DERMAL HYPOPLASIA 1985-92 ,do not confuse entry term GOLTZ-GORLIN SYNDROME with GORLIN-GOLTZ SYNDROME see BASAL CELL NEVUS SYNDROME ,use FOCAL DERMAL HYPOPLASIA to search GOLTZ-GORLIN SYNDROME 1985-92
D005489