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9 entries on 1 page. Showing entries 1 - 9.

ID     

AscendingAbbreviation     

Name     

OMIM ID     

Individuals     

Phenotypes     

Associated with genes
00007 AI hypocal.mat. Amelogenesis Imperfecta - hypocalcified hypomaturation - 0 0 -
00005 AI hypocalc. Amelogenesis Imperfecta - hypocalcified - 48 50 FAM83H
00001 AI hypomat. Amelogenesis Imperfecta - hypomaturation - 52 50 AMELX, GPR68, KLK4, MMP20, SLC24A4, WDR72
00004 AI hypomin. Amelogenesis Imperfecta - hypomineralised - 12 13 AMELX, AMTN, C4orf26, FAM83H, ITGB6, SLC24A4
00006 AI hypomin.mat Amelogenesis Imperfecta - hypomineralised hypomaturation - 4 4 GPR68
00003 AI hypopla.mat. Amelogenesis Imperfecta - hypoplastic hypomaturation - 9 9 AMELX, COL17A1, DLX3
00008 AI hypopla.min. Amelogenesis Imperfecta - hypoplastic hypomineralised - 7 7 AMELX, WDR72
00002 AI hypoplastic Amelogenesis Imperfecta - hypoplastic - 133 133 ACPT, AMBN, AMELX, COL17A1, ENAM, FAM20A, ITGB6, LAMA3, LAMB3, RELT, SP6
00009 AI unclassified Amelogenesis imperfecta - not classified - 12 12 -