All diseases

OMIM ID
309800
OMIM term:
MICROPHTHALMIA, SYNDROMIC 1; MCOPS1
Alternative terms:
LENZ MICROPHTHALMIA SYNDROME
LENZ DYSPLASIA
MAA, FORMERLY
(∗) Location:
Xq27-q28  
(†) Associated OMIM genes:
(‡) Associated MGI genes:

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