Concept information
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Genetic Diseases, Inborn
Genetic Diseases, X-Linked
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Congenital Abnormalities
Abnormalities, Multiple
Ectodermal Dysplasia
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Genetic Diseases, Inborn
Skin Diseases, Genetic
Ectodermal Dysplasia
Término preferido
Focal Dermal Hypoplasia
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Tipo
-
mesh:Descriptor
Definición
- 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.
Concepto genérico
Etiquetas alternativas
- Dermal Hypoplasia, Focal
- Goltz Gorlin Syndrome
- Goltz Syndrome
- Goltz-Gorlin Syndrome
- Goltz's Syndrome
En otras lenguas
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francés
-
Hypoplasie dermique focale
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Syndrome de Goltz
-
Syndrome de Goltz-Gorlin
URI
http://data.loterre.fr/ark:/67375/JVR-TPC7BCZB-K
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