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Core Information
Disease Name
Gorlin Syndrome
Standard Disease Name
gorlin syndrome
MeSH Tree
No data
ICD-10
Q87.8
Identifiers
DO ID
No data
MeSH ID
No data
OMIM ID
109400
UMLS ID
C0812437|C0004779
HPO ID
No data
Description and Extensions
Description
Gorlin syndrome (GS) is a genodermatosis characterized by multiple early-onset basal cell carcinoma (BCC), odontogenic keratocysts and skeletal abnormalities.
Related
Related Entities
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