All diseases

OMIM ID
108300
OMIM term:
STICKLER SYNDROME, TYPE I; STL1
Alternative terms:
STICKLER SYNDROME, VITREOUS TYPE 1
STICKLER SYNDROME, MEMBRANOUS VITREOUS TYPE
ARTHROOPHTHALMOPATHY, HEREDITARY PROGRESSIVE; AOM
(∗) Location:
12q13.11  
(†) Associated OMIM genes:
COL2A1  
(‡) Associated MGI genes:

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