All diseases

OMIM ID
213300
OMIM term:
JOUBERT SYNDROME; JBTS
Alternative terms:
JOUBERT-BOLTSHAUSER SYNDROME
CEREBELLOPARENCHYMAL DISORDER IV; CPD4 JOUBERT SYNDROME 1, INCLUDED; JBTS1, INCLUDED
CEREBELLOOCULORENAL SYNDROME 1, INCLUDED; CORS1, INCLUDED
(∗) Location:
9q34.3  
(†) Associated OMIM genes:
INPP5E  
(‡) Associated MGI genes:
Zic1   b2b012Clo  

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