All diseases

OMIM ID
109400
OMIM term:
BASAL CELL NEVUS SYNDROME; BCNS
Alternative terms:
GORLIN SYNDROME
GORLIN-GOLTZ SYNDROME
NEVOID BASAL CELL CARCINOMA SYNDROME; NBCCS
MULTIPLE BASAL CELL NEVI, ODONTOGENIC KERATOCYSTS, AND SKELETAL ANOMALIES
(∗) Location:
9q22.32  
(†) Associated OMIM genes:
PTCH1  
(‡) Associated MGI genes:
Ptch1   Sufu  

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* quick link - http://q.sanger.ac.uk/v95pi5dc