Nevoid basal cell carcinoma syndrome
MONDO:0007187A rare hereditary disorder due to autosomal dominant transmission with hamartosis characterized by multiple early-onset basal cell carcinoma (BCC), multiple jaw keratocysts and skeletal abnormalities.
Also known as: Gorlin syndrome, Gorlin-Goltz syndrome, NBCCS, basal cell nevus syndrome, multiple basal cell carcinomas, nevoid basal cell cancer syndrome, nevoid basal cell carcinoma syndrome, BCNS
36 clinical trials for this condition and its sub-types.
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Broader categories
Disease
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Nervous system disorder
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Hereditary disease
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Inherited disease susceptibility
(79)
Hereditary neoplastic syndrome
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Syndromic disease
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Human disease
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Developmental defect during embryogenesis
(8)
Neoplastic disease or syndrome
(7)
Hereditary neurological disease
(6)