All diseases

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

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
04116 MCSKS;MCOPS14 Microphthalmia/coloboma and skeletal dysplasia syndrome 615877 AD;AR - - MAB21L2 - -
00402 OCCO coloboma, ocular (OCCO) - - 9 9 MAB21L2 - -
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