Phenotypes for disease #02344 (MCOPS9 (microphthalmia syndromic, type 9 (MCOPS-9)), OMIM:601186)

2 entries on 1 page. Showing entries 1 - 2.
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AscendingPhenotype ID     

Phenotype details     

Diagnosis/Initial     

Diagnosis/Definite     

Inheritance     

Age/Examination     

Age/Diagnosis     

Age/Onset     

Phenotype/Onset     

Protein     

Owner     

Individual ID     
0000275931 microphthalmia, anophthalmia, and coloboma; MIM, 601186 MIM, 601186 - Familial, autosomal recessive - - - - - LOVD 00382089
0000275991 congenital cataract; MIM, 600897 MIM, 600897 - Familial, autosomal dominant - - - - - LOVD 00382149
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