- OMIM ID
-
300166
- OMIM term:
- MICROPHTHALMIA, SYNDROMIC 2; MCOPS2
- Alternative terms:
-
OCULOFACIOCARDIODENTAL SYNDROME
OFCD SYNDROME
MICROPHTHALMIA, CATARACTS, RADICULOMEGALY, AND SEPTAL HEART DEFECTS
ANOP2, FORMERLY
MAA2, FORMERLY
- (∗) Location:
- Xp11.4
- (†) Associated OMIM genes:
- BCOR
- (‡) Associated MGI genes:
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