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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 |
|---|---|---|---|---|---|
| C0040034 | Thrombocytopenia | TALDO1 | 6888 | transaldolase 1 | P37837 |
| C0004096 | Asthma | TALDO1 | 6888 | transaldolase 1 | P37837 |
| C0235991 | Small for gestational age (disorder) | TALDO1 | 6888 | transaldolase 1 | P37837 |
| C0007137 | Squamous cell carcinoma | TALDO1 | 6888 | transaldolase 1 | P37837 |
| C0007114 | Malignant neoplasm of skin | TALDO1 | 6888 | transaldolase 1 | P37837 |
| C1168401 | Squamous cell carcinoma of the head and neck | TALDO1 | 6888 | transaldolase 1 | P37837 |
| C0035579 | Rickets | TALDO1 | 6888 | transaldolase 1 | P37837 |
| C0039446 | Telangiectasis | TALDO1 | 6888 | transaldolase 1 | P37837 |
| C0025517 | Metabolic Diseases | TALDO1 | 6888 | transaldolase 1 | P37837 |
| C0043346 | Xeroderma Pigmentosum | TALDO1 | 6888 | transaldolase 1 | P37837 |
| C0239946 | Fibrosis, Liver | TALDO1 | 6888 | transaldolase 1 | P37837 |
| C0011847 | Diabetes | TALDO1 | 6888 | transaldolase 1 | P37837 |
| C0011053 | Deafness | TALDO1 | 6888 | transaldolase 1 | P37837 |
| C0016522 | Foramen Ovale, Patent | TALDO1 | 6888 | transaldolase 1 | P37837 |
| C0002895 | Anemia, Sickle Cell | TALDO1 | 6888 | transaldolase 1 | P37837 |
| C0011849 | Diabetes Mellitus | TALDO1 | 6888 | transaldolase 1 | P37837 |
| C0018818 | Ventricular Septal Defects | TALDO1 | 6888 | transaldolase 1 | P37837 |
| C0268419 | Acatalasia | TALDO1 | 6888 | transaldolase 1 | P37837 |
| C2931868 | Catalase deficiency | TALDO1 | 6888 | transaldolase 1 | P37837 |
| C0030481 | Tropical Spastic Paraparesis | CNTN2 | 6900 | contactin 2 | Q02246 |
| C0234533 | Generalized seizures | CNTN2 | 6900 | contactin 2 | Q02246 |
| C0002395 | Alzheimer's Disease | CNTN2 | 6900 | contactin 2 | Q02246 |
| C0004364 | Autoimmune Diseases | CNTN2 | 6900 | contactin 2 | Q02246 |
| C0023492 | Leukemia, T-Cell | CNTN2 | 6900 | contactin 2 | Q02246 |
| C0005684 | Malignant neoplasm of urinary bladder | CNTN2 | 6900 | contactin 2 | Q02246 |
