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Congenital, Hereditary, and Neonatal Diseases and Abnormalities > Genetic Diseases, Inborn > Genetic Diseases, X-Linked > Focal Dermal Hypoplasia
Congenital, Hereditary, and Neonatal Diseases and Abnormalities > Congenital Abnormalities > Abnormalities, Multiple > Ectodermal Dysplasia > Focal Dermal Hypoplasia
Congenital, Hereditary, and Neonatal Diseases and Abnormalities > Genetic Diseases, Inborn > Skin Diseases, Genetic > Ectodermal Dysplasia > Focal Dermal Hypoplasia
Skin and Connective Tissue Diseases > Skin Diseases > Skin Diseases, Genetic > Ectodermal Dysplasia > Focal Dermal Hypoplasia
Skin and Connective Tissue Diseases > Skin Diseases > Skin Abnormalities > Ectodermal Dysplasia > Focal Dermal Hypoplasia
Congenital, Hereditary, and Neonatal Diseases and Abnormalities > Congenital Abnormalities > Skin Abnormalities > Ectodermal Dysplasia > Focal Dermal Hypoplasia
Musculoskeletal Diseases > Bone Diseases > Bone Diseases, Developmental > Dysostoses > Focal Dermal Hypoplasia

Preferred term

Focal Dermal Hypoplasia  

Type

  • mesh:Descriptor

Definition

  • 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.

Broader concept

Entry terms

  • Dermal Hypoplasia, Focal
  • Goltz Gorlin Syndrome
  • Goltz-Gorlin Syndrome
  • Goltz's Syndrome
  • Goltz Syndrome

Allowable Qualifier(s)

In other languages

URI

http://data.loterre.fr/ark:/67375/JVR-TPC7BCZB-K

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RDF/XML TURTLE JSON-LD Created 4/5/84, last modified 6/18/15