- OMIM ID
-
607932
- OMIM term:
- MICROPHTHALMIA, SYNDROMIC 6; MCOPS6
- Alternative terms:
-
MICROPHTHALMIA AND PITUITARY ANOMALIES
MICROPHTHALMIA WITH BRAIN AND DIGIT DEVELOPMENTAL ANOMALIES
ANOPHTHALMIA, CLINICAL, WITH MICROGNATHIA, MALFORMED EARS, DIGITAL ANOMALIES, AND ABNORMAL EXTERNAL GENITALIA
- (∗) Location:
- 14q22.2
- (†) Associated OMIM genes:
- BMP4
- (‡) Associated MGI genes:
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