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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 |
|---|---|---|---|---|---|
| C0035204 | Respiration Disorders | SFTPA2 | 729238 | surfactant protein A2 | Q8IWL1 |
| C0243026 | Sepsis | SFTPA2 | 729238 | surfactant protein A2 | Q8IWL1 |
| C0004153 | Atherosclerosis | SFTPA2 | 729238 | surfactant protein A2 | Q8IWL1 |
| C4721952 | Familial Idiopathic Pulmonary Fibrosis | SFTPA2 | 729238 | surfactant protein A2 | Q8IWL1 |
| C1855179 | CATARACT, ANTERIOR POLAR | SFTPA2 | 729238 | surfactant protein A2 | Q8IWL1 |
| C0262655 | Recurrent urinary tract infection | SFTPA2 | 729238 | surfactant protein A2 | Q8IWL1 |
| C1535939 | Pneumocystis jiroveci pneumonia | SFTPA2 | 729238 | surfactant protein A2 | Q8IWL1 |
| C0006826 | Malignant Neoplasms | SFTPA2 | 729238 | surfactant protein A2 | Q8IWL1 |
| C0017168 | Gastroesophageal reflux disease | SFTPA2 | 729238 | surfactant protein A2 | Q8IWL1 |
| C0264490 | Acute respiratory failure | SFTPA2 | 729238 | surfactant protein A2 | Q8IWL1 |
| C4721508 | Hamman-Rich Disease | SFTPA2 | 729238 | surfactant protein A2 | Q8IWL1 |
| C0020459 | Hyperinsulinism | SFTPA2 | 729238 | surfactant protein A2 | Q8IWL1 |
| C0029882 | Otitis Media | SFTPA2 | 729238 | surfactant protein A2 | Q8IWL1 |
| C0085786 | Hamman-Rich syndrome | SFTPA2 | 729238 | surfactant protein A2 | Q8IWL1 |
| C0007137 | Squamous cell carcinoma | SFTPA2 | 729238 | surfactant protein A2 | Q8IWL1 |
| C0017636 | Glioblastoma | TPI1 | 7167 | triosephosphate isomerase 1 | P60174 |
| C0027651 | Neoplasms | TPI1 | 7167 | triosephosphate isomerase 1 | P60174 |
| C0002878 | Anemia, Hemolytic | TPI1 | 7167 | triosephosphate isomerase 1 | P60174 |
| C0025517 | Metabolic Diseases | TPI1 | 7167 | triosephosphate isomerase 1 | P60174 |
| C0003850 | Arteriosclerosis | TPI1 | 7167 | triosephosphate isomerase 1 | P60174 |
| C0699791 | Stomach Carcinoma | TPI1 | 7167 | triosephosphate isomerase 1 | P60174 |
| C1510586 | Autism Spectrum Disorders | TPI1 | 7167 | triosephosphate isomerase 1 | P60174 |
| C0002395 | Alzheimer's Disease | TPI1 | 7167 | triosephosphate isomerase 1 | P60174 |
| C0027765 | nervous system disorder | TPI1 | 7167 | triosephosphate isomerase 1 | P60174 |
| C1860808 | Triosephosphate Isomerase Deficiency | TPI1 | 7167 | triosephosphate isomerase 1 | P60174 |
