Disease #00051 (T2D (TYPE 2 DIABETES MELLITUS), OMIM:125853)
| Official abbreviation |
T2D |
| Name |
TYPE 2 DIABETES MELLITUS |
| OMIM ID |
125853 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
Autosomal dominant |
| Individuals reported having this disease |
- |
| Phenotype entries for this disease |
- |
| Associated with 6 genes |
ABCC8, GCK, HNF1A, HNF4A, NEUROD1, PAX4 |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2020-03-03 14:34:43 +00:00 (UTC) |
| Date last edited |
2023-06-16 09:21:50 +00:00 (UTC) |
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