Concept information
Término preferido
Corneal Dystrophy, Juvenile Epithelial of Meesmann
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Tipo
-
mesh:Descriptor
Definición
- An autosomal dominant form of hereditary corneal dystrophy due to a defect in cornea-specific KERATIN formation. Mutations in the genes that encode KERATIN-3 and KERATIN-12 have been linked to this disorder.
Concepto genérico
Etiquetas alternativas
- Corneal Dystrophy, Meesmann
- Corneal Dystrophy, Meesmann Epithelial
- Juvenile Hereditary Epithelial Dystrophy
- Meesmann Corneal Dystrophy
- Meesmann Corneal Epithelial Dystrophy
- Meesmann Epithelial Corneal Dystrophy
En otras lenguas
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francés
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Dystrophie cornéenne épithéliale juvénile de Meesmann
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Dystrophie de Meesmann
URI
http://data.loterre.fr/ark:/67375/JVR-R4GGXMB1-C
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