- OMIM ID
-
186580
- OMIM term:
- BLAU SYNDROME
- Alternative terms:
-
GRANULOMATOSIS, FAMILIAL JUVENILE SYSTEMIC
ARTHROCUTANEOUVEAL GRANULOMATOSIS; ACUG
JABS SYNDROME
GRANULOMATOUS INFLAMMATORY ARTHRITIS, DERMATITIS, AND UVEITIS, FAMILIAL
GRANULOMATOSIS, FAMILIAL, BLAU TYPE SYNOVITIS, GRANULOMATOUS, WITH UVEITIS AND CRANIAL NEUROPATHIES, INCLUDED
- (∗) Location:
- 16q12.1
- (†) Associated OMIM genes:
- NOD2
- (‡) Associated MGI genes:
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