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 |
- |
| Date created |
2013-06-14 15:56:30 +02:00 (CEST) |
| Date last edited |
2021-12-10 21:51:32 +01:00 (CET) |
Individuals
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