Concept information
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Congenital Abnormalities
Abnormalities, Multiple
...
Neoplasms by Histologic Type
Neoplasms, Glandular and Epithelial
Carcinoma
Carcinoma, Basal Cell
...
Neoplasms by Histologic Type
Neoplasms, Glandular and Epithelial
Neoplasms, Basal Cell
Carcinoma, Basal Cell
Término preferido
Basal Cell Nevus Syndrome
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Tipo
-
mesh:Descriptor
Definición
- Hereditary disorder consisting of multiple basal cell carcinomas, odontogenic keratocysts, and multiple skeletal defects, e.g., frontal and temporoparietal bossing, bifurcated and splayed ribs, kyphoscoliosis, fusion of vertebrae, and cervicothoracic spina bifida. Genetic transmission is autosomal dominant.
Concepto genérico
Etiquetas alternativas
- Fifth Phacomatosis
- Gorlin Syndrome
- Gorlin-Goltz Syndrome
- Multiple Basal Cell Nevi, Odontogenic Keratocysts, and Skeletal Anomalies
- NBCCS
- Nevoid Basal Cell Carcinoma Syndrome
- Nevus Syndrome, Basal Cell
En otras lenguas
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francés
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Cinquième phacomatose
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Naevomatose baso-cellulaire
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NBC (Naevomatose BasoCellulaire)
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Syndrome de carcinome basocellulaire naevoïde
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Syndrome de Gorlin
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Syndrome de Gorlin-Goltz
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Syndrome du carcinome naevoïde basocellulaire
URI
http://data.loterre.fr/ark:/67375/JVR-SFKB6GND-C
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