- OMIM ID
-
601186
- OMIM term:
- MICROPHTHALMIA, SYNDROMIC 9; MCOPS9
- Alternative terms:
-
ANOPHTHALMIA, CLINICAL, WITH MILD FACIAL DYSMORPHISM AND VARIABLE MALFORMATIONS OF THE LUNG, HEART, AND DIAPHRAGM
ANOPHTHALMIA/MICROPHTHALMIA AND PULMONARY HYPOPLASIA
SPEAR SYNDROME
MATTHEW-WOOD SYNDROME
PULMONARY AGENESIS, MICROPHTHALMIA, AND DIAPHRAGMATIC DEFECT; PMD
- (∗) Location:
- 15q24.1
- (†) Associated OMIM genes:
- STRA6
- (‡) Associated MGI genes:
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