All diseases

3 entries on 1 page. Showing entries 1 - 3.
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ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
00154 KNO2 Knobloch syndrome, type 2 (KNO-2) 608454 - 1 1 ADAMTS18 - -
00155 MMCAT microcornea, myopic chorioretinal atrophy and telecanthus (MMCAT) - - 4 - ADAMTS18 - -
03956 MMCAT microcornea, myopic chorioretinal atrophy, and telecanthus 615458 AR - - ADAMTS18 - -
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