microphthalmia, syndromic, type 9
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microphthalmia, syndromic, type 9A clinically heterogeneous disorder (OMIM:601186) of eye formation, ranging from unilateral microphthalmia to bilateral anophthalmia, which may be associated with pulmonary hypoplasia or aplasia.
Caused by defects of STRA6, which encodes a membrane protein involved in retinol metabolism.
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