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DisGeNET
DisGeNET is a knowledge management platform that integrates and standardizes the data of genes and mutations related to diseases from multiple sources. It covers entire range of human disease.
| Source | Last Updated |
|---|---|
| DisGeNET | July 29, 2024 |
| Disease ID | Disease Name | Gene Symbol ▲ | Gene ID | Gene Name | UniProt ID |
|---|---|---|---|---|---|
| C0019158 | Hepatitis | PGM1 | 5236 | phosphoglucomutase 1 | P36871 |
| C0024530 | Malaria | PGM1 | 5236 | phosphoglucomutase 1 | P36871 |
| C2239176 | Liver carcinoma | PGM1 | 5236 | phosphoglucomutase 1 | P36871 |
| C0009402 | Colorectal Carcinoma | PGM1 | 5236 | phosphoglucomutase 1 | P36871 |
| C0000768 | Congenital Abnormality | PGM1 | 5236 | phosphoglucomutase 1 | P36871 |
| C0007959 | Charcot-Marie-Tooth Disease | PGM1 | 5236 | phosphoglucomutase 1 | P36871 |
| C0024141 | Lupus Erythematosus, Systemic | PGM1 | 5236 | phosphoglucomutase 1 | P36871 |
| C3808991 | NGLY1 deficiency | PGM1 | 5236 | phosphoglucomutase 1 | P36871 |
| C3888018 | Congenital Hyperinsulinism | PGM1 | 5236 | phosphoglucomutase 1 | P36871 |
| C0525045 | Mood Disorders | PGM1 | 5236 | phosphoglucomutase 1 | P36871 |
| C0003811 | Cardiac Arrhythmia | PGM1 | 5236 | phosphoglucomutase 1 | P36871 |
| C0007193 | Cardiomyopathy, Dilated | PGM1 | 5236 | phosphoglucomutase 1 | P36871 |
| C0678213 | Complete hydatidiform mole | PGM1 | 5236 | phosphoglucomutase 1 | P36871 |
| C0003872 | Arthritis, Psoriatic | PGM1 | 5236 | phosphoglucomutase 1 | P36871 |
| C0027651 | Neoplasms | PGM1 | 5236 | phosphoglucomutase 1 | P36871 |
| C0037274 | Dermatologic disorders | PGM1 | 5236 | phosphoglucomutase 1 | P36871 |
| C3887645 | Job Syndrome | PGM3 | 5238 | phosphoglucomutase 3 | O95394 |
| C0029422 | Osteochondrodysplasias | PGM3 | 5238 | phosphoglucomutase 3 | O95394 |
| C0021051 | Immunologic Deficiency Syndromes | PGM3 | 5238 | phosphoglucomutase 3 | O95394 |
| C0036572 | Seizures | PGM3 | 5238 | phosphoglucomutase 3 | O95394 |
| C0013595 | Eczema | PGM3 | 5238 | phosphoglucomutase 3 | O95394 |
| C0018784 | Sensorineural Hearing Loss (disorder) | PGM3 | 5238 | phosphoglucomutase 3 | O95394 |
| C2936739 | Hyper-Immunoglobulin E Syndrome, Autosomal Dominant | PGM3 | 5238 | phosphoglucomutase 3 | O95394 |
| C0085110 | Severe Combined Immunodeficiency | PGM3 | 5238 | phosphoglucomutase 3 | O95394 |
| C0024299 | Lymphoma | PGM3 | 5238 | phosphoglucomutase 3 | O95394 |
