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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 |
|---|---|---|---|---|---|
| C1961835 | Gaucher Disease, Type 1 | PSAP | 5660 | prosaposin | P07602 |
| C0008489 | Chorea | PSAP | 5660 | prosaposin | P07602 |
| C0006849 | Oral candidiasis | PSAP | 5660 | prosaposin | P07602 |
| C0266999 | Vesicular Stomatitis | PSAP | 5660 | prosaposin | P07602 |
| C0751276 | Metachromatic leukodystrophy, juvenile type | PSAP | 5660 | prosaposin | P07602 |
| C0494475 | Tonic - clonic seizures | PSAP | 5660 | prosaposin | P07602 |
| C0919267 | ovarian neoplasm | PSAP | 5660 | prosaposin | P07602 |
| C0264408 | Childhood asthma | PSAP | 5660 | prosaposin | P07602 |
| C0235782 | Gallbladder Carcinoma | PSAP | 5660 | prosaposin | P07602 |
| C2239176 | Liver carcinoma | PSAP | 5660 | prosaposin | P07602 |
| C0016057 | Fibrosarcoma | PSAP | 5660 | prosaposin | P07602 |
| C1306459 | Primary malignant neoplasm | PSAP | 5660 | prosaposin | P07602 |
| C1136084 | Plasma cell dyscrasia | PSAP | 5660 | prosaposin | P07602 |
| C0233844 | Clumsiness | PSAP | 5660 | prosaposin | P07602 |
| C0006840 | Candidiasis | PSAP | 5660 | prosaposin | P07602 |
| C0268255 | Farber Lipogranulomatosis | PSAP | 5660 | prosaposin | P07602 |
| C0036572 | Seizures | PSAP | 5660 | prosaposin | P07602 |
| C0153252 | Systemic candidiasis | PSAP | 5660 | prosaposin | P07602 |
| C0030486 | Paraplegia | PSAP | 5660 | prosaposin | P07602 |
| C3714731 | Early childhood caries | PSAP | 5660 | prosaposin | P07602 |
| C0006846 | Cutaneous Candidiasis | PSAP | 5660 | prosaposin | P07602 |
| C0019693 | HIV Infections | PSAP | 5660 | prosaposin | P07602 |
| C0278595 | Adult Fibrosarcoma | PSAP | 5660 | prosaposin | P07602 |
| C0699791 | Stomach Carcinoma | PSAP | 5660 | prosaposin | P07602 |
| C0029124 | Optic Atrophy | PSAP | 5660 | prosaposin | P07602 |
