All diseases

OMIM ID
600975
OMIM term:
GLAUCOMA 3, PRIMARY INFANTILE, B; GLC3B
Alternative terms:
GLAUCOMA, PRIMARY CONGENITAL, TYPE B
GLC3, TYPE B
(∗) Location:
1p36.2-p36.1  
(†) Associated OMIM genes:
(‡) Associated MGI genes:

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