All diseases

4 entries on 1 page. Showing entries 1 - 4.
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ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
02331 GLC3B glaucoma, congenital, primary infantile, type 3B (GLC-3B) 600975 - 1 1 CYP1B1, LTBP2 - -
03246 GLC3D glaucoma, congenital, primary, type 3D (GLC-3D) 613086 - 21 19 LTBP2 - -
01924 MSPKA microspherophakia and/or megalocornea, with ectopia lentis, with/without secondary glaucoma (MSPKA) 251750 AR 7 7 LTBP2 - -
03734 WMS3 Weill-Marchesani syndrome, type 3 (WMS-3) 614819 AR 1 1 LTBP2 - -
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