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DeCS
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Descriptor English:
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Basal Cell Nevus Syndrome
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Descriptor Spanish:
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Síndrome del Nevo Basocelular
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Descriptor Portuguese:
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Síndrome do Nevo Basocelular
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Synonyms English:
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Gorlin Syndrome
Nevoid Basal Cell Carcinoma Syndrome
Nevus Syndrome, Basal Cell
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Tree Number:
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C04.182.089.530.690.150
C04.557.470.200.165.150
C04.557.470.565.165.150
C04.700.175
C05.116.099.105
C05.500.470.690.150
C07.320.450.670.130
C16.131.077.130
C16.320.700.175
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Definition English:
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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. |
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Indexing Annotation English:
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coord IM with precoord organ/neopl (IM or NIM) only if pertinent; do not confuse X ref GORLIN SYNDROME (also called Gorlin-Goltz syndrome) with GOLTZ SYNDROME see FOCAL DERMAL HYPOPLASIA
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History Note English:
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91(80); was see under CARCINOMA, BASAL CELL 1980-90
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Allowable Qualifiers English:
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Record Number:
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23952
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Unique Identifier:
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D001478
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Occurrence in VHL:
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Similar:
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DeCS SciELO LILACS LIS
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