Structured Summary
Abstract
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.
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Classification
Broader headings
Related Concepts
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MeSH Record
Synonyms
15 entry terms
- Dermal Hypoplasia, Focal
- Goltz Gorlin Syndrome
- Goltz Syndrome
- Goltz's Syndrome
- Goltz-Gorlin Syndrome
- Dermal Hypoplasias, Focal
- Focal Dermal Hypoplasias
- Goltzs Syndrome
- Gorlin Syndrome, Goltz
- Hypoplasia, Focal Dermal
- Hypoplasias, Focal Dermal
- Syndrome, Goltz
- Syndrome, Goltz Gorlin
- Syndrome, Goltz's
- Syndrome, Goltz-Gorlin
MeSH Record
Aspects Covered
34 allowable subheadings
Indexed with the subheadings blood, cerebrospinal fluid, chemically induced, classification, complications, diagnosis, diagnostic imaging, diet therapy, drug therapy, economics, embryology, enzymology, epidemiology, ethnology, etiology, genetics, history, immunology, metabolism, microbiology, mortality, nursing, parasitology, pathology, physiopathology, prevention & control, psychology, radiotherapy, rehabilitation, surgery, therapy, urine, veterinary, virology.
MeSH Record
Indexing Annotation
do not confuse entry term GOLTZ-GORLIN SYNDROME with GORLIN-GOLTZ SYNDROME see BASAL CELL NEVUS SYNDROME
MeSH Record
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
MeSH Record
Previous Indexing
- Abnormalities, Multiple (1968-1984)
- Skin (1966-1984)
- Skin Diseases (1966-1984)
MeSH Hierarchy
Tree Numbers
AMA Style
References
- National Library of Medicine. Focal Dermal Hypoplasia. Medical Subject Headings (MeSH). 2026. Unique ID D005489. http://id.nlm.nih.gov/mesh/2026/D005489
- Focal Dermal Hypoplasia. In: Wikipedia. https://en.wikipedia.org/wiki/Focal_dermal_hypoplasia
- Focal Dermal Hypoplasia. In: Wikidata. https://www.wikidata.org/wiki/Q5463847