Syndromic microphthalmia type 5

Syndromic microphthalmia, type 5 is characterized by the association of a range of ocular anomalies (anophthalmia, microphthalmia and retinal abnormalities) with variable developmental delay and central nervous system malformations.

Also known as: MCOPS5, OTX2 syndromic microphthalmia, microphthalmia, syndromic type 5, syndromic microphthalmia caused by mutation in OTX2, syndromic microphthalmia type 5, syndromic microphthalmia/anophthalmia due to OTX2 mutation, OTX2-related eye disorders, microphthalmia syndromic 5

0 clinical trials for this condition and its sub-types, 0 tagged with Syndromic microphthalmia type 5 itself.