Disease #00151 (NIDDM (diabetes mellitus, type II (NIDDM)), OMIM:125853)
Official abbreviation |
NIDDM |
Name |
diabetes mellitus, type II (NIDDM) |
OMIM ID |
125853 |
Human Phenotype Ontology Project (HPO) |
HPO |
Inheritance |
Autosomal dominant |
Individuals reported having this disease |
8 |
Phenotype entries for this disease |
7 |
Associated with 28 genes |
ABCC8, AKT2, CDKAL1, ENPP1, GCGR, GCK, GPD2, HMGA1, HNF1A, HNF1B, HNF4A, IGF2BP2, IRS1, IRS2, KCNJ11, LIPC, MAPK8IP1, MTNR1B, NEUROD1, PAX4, 8 more...ABCC8, AKT2, CDKAL1, ENPP1, GCGR, GCK, GPD2, HMGA1, HNF1A, HNF1B, HNF4A, IGF2BP2, IRS1, IRS2, KCNJ11, LIPC, MAPK8IP1, MTNR1B, NEUROD1, PAX4, PDX1, PPARG, PTPN1, RETN, SLC2A2, SLC30A8, TCF7L2, WFS1 |
Associated tissues |
- |
Disease features |
- |
Remarks |
- |
Individuals
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