- OMIM ID
-
301590
- OMIM term:
- MICROPHTHALMIA, SYNDROMIC 4; MCOPS4
- Alternative terms:
-
MICROPHTHALMIA WITH ANKYLOBLEPHARON AND MENTAL RETARDATION
ANOP1, FORMERLY
- (∗) Location:
- Xq27-q28
- (†) Associated OMIM genes:
- (‡) Associated MGI genes:
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