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Focal Dermal Hypoplasia MeSH Descriptor Data 2022


MeSH Heading
Focal Dermal Hypoplasia
Tree Number(s)
C05.116.099.370.380
C16.131.077.350.424
C16.131.831.350.424
C16.320.322.186
C16.320.850.250.424
C17.800.804.350.424
C17.800.827.250.424
Unique ID
D005489
RDF Unique Identifier
http://id.nlm.nih.gov/mesh/D005489
Annotation
do not confuse entry term GOLTZ-GORLIN SYNDROME with GORLIN-GOLTZ SYNDROME see BASAL CELL NEVUS SYNDROME
Scope Note
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.
Entry Term(s)
Dermal Hypoplasia, Focal
Goltz Gorlin Syndrome
Goltz Syndrome
Goltz's Syndrome
Goltz-Gorlin Syndrome
Previous Indexing
Abnormalities, Multiple (1968-1984)
Skin (1966-1984)
Skin Diseases (1966-1984)
Public MeSH Note
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
Online Note
use FOCAL DERMAL HYPOPLASIA to search GOLTZ-GORLIN SYNDROME 1985-92
History Note
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
Date Established
1991/01/01
Date of Entry
1984/04/05
Revision Date
2015/06/18
Focal Dermal Hypoplasia Preferred
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