All diseases

OMIM ID
309801
OMIM term:
MICROPHTHALMIA, SYNDROMIC 7; MCOPS7
Alternative terms:
MICROPHTHALMIA WITH LINEAR SKIN DEFECTS; MLS
MICROPHTHALMIA, DERMAL APLASIA, AND SCLEROCORNEA
MIDAS SYNDROME
(∗) Location:
Xp22.2  
(†) Associated OMIM genes:
HCCS  
(‡) Associated MGI genes:

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