- OMIM ID
-
206900
- OMIM term:
- MICROPHTHALMIA, SYNDROMIC 3; MCOPS3
- Alternative terms:
-
MICROPHTHALMIA AND ESOPHAGEAL ATRESIA SYNDROME
ANOPHTHALMIA, CLINICAL, WITH ASSOCIATED ANOMALIES
ANOPHTHALMIA-ESOPHAGEAL-GENITAL SYNDROME
AEG SYNDROME OPTIC NERVE HYPOPLASIA AND ABNORMALITIES OF THE CENTRAL NERVOUS SYSTEM, INCLUDED
- (∗) Location:
- 3q26.33
- (†) Associated OMIM genes:
- SOX2
- (‡) Associated MGI genes:
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