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
03307 ARHR2 rickets, hypophosphatemic, autosomal recessive, type 2 (ARHR-2) 613312 AR 4 4 ENPP1 - -
03985 COLED Cole disease (COLED) 615522 AD - - ENPP1 - -
01664 GACI1 calcification, arterial, generalized, infancy, type 1 (GACI-1) 208000 AR 49 48 ENPP1 - -
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 - -
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