All diseases

5 entries on 1 page. Showing entries 1 - 5.
Legend   How to query  

ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
01237 CTRCT41 cataract, type 41 (CTRCT-41, congenital nuclear type) 116400 AD 0 0 WFS1 - -
02327 DFNA6 Deafness, autosomal dominant, type A6 600965 AD 0 0 WFS1 - -
00151 NIDDM diabetes mellitus, type II (NIDDM) 125853 AD 8 7 ABCC8, AKT2, CDKAL1, ENPP1, GCGR, GCK, GPD2, HMGA1, HNF1A, HNF1B, HNF4A, IGF2BP2, IRS1, IRS2, KCNJ11, LIPC, MAPK8IP1, MTNR1B, NEUROD1, PAX4, 8 more - -
01750 WFS1 Wolfram syndrome, type 1 (WFS1) 222300 AR 0 0 WFS1 - -
03596 WFSL Wolfram-like syndrome, autosomal dominant (WFSL) 614296 AD 1 1 WFS1 - -
Legend   How to query