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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 ▲ |
|---|---|---|---|---|---|
| C0085078 | Lysosomal Storage Diseases | PSAP | 5660 | prosaposin | P07602 |
| C0376358 | Malignant neoplasm of prostate | PSAP | 5660 | prosaposin | P07602 |
| C0268262 | Metachromatic Leukodystrophy due to Saposin B Deficiency | PSAP | 5660 | prosaposin | P07602 |
| C0015652 | Fascioliasis | PSAP | 5660 | prosaposin | P07602 |
| C0026650 | Movement Disorders | PSAP | 5660 | prosaposin | P07602 |
| C0243026 | Sepsis | PSAP | 5660 | prosaposin | P07602 |
| C0023521 | Globoid cell leukodystrophy | PSAP | 5660 | prosaposin | P07602 |
| C0027651 | Neoplasms | PSAP | 5660 | prosaposin | P07602 |
| C0000768 | Congenital Abnormality | PSAP | 5660 | prosaposin | P07602 |
| C0027877 | Neuronal Ceroid-Lipofuscinoses | PSAP | 5660 | prosaposin | P07602 |
| C0023522 | Leukodystrophy, Metachromatic | PSAP | 5660 | prosaposin | P07602 |
| C0152025 | Polyneuropathy | PSAP | 5660 | prosaposin | P07602 |
| C0024530 | Malaria | PSAP | 5660 | prosaposin | P07602 |
| C0678222 | Breast Carcinoma | PSAP | 5660 | prosaposin | P07602 |
| C0023524 | Leukoencephalopathy, Progressive Multifocal | PSAP | 5660 | prosaposin | P07602 |
| C0006142 | Malignant neoplasm of breast | PSAP | 5660 | prosaposin | P07602 |
| C0404521 | Infective vaginitis | PSAP | 5660 | prosaposin | P07602 |
| C1458155 | Mammary Neoplasms | PSAP | 5660 | prosaposin | P07602 |
| C0006852 | Candidiasis of vagina | PSAP | 5660 | prosaposin | P07602 |
| C0008325 | Cholecystitis | PSAP | 5660 | prosaposin | P07602 |
| C0751279 | Metachromatic Leukodystrophy, Adult-Type (disorder) | PSAP | 5660 | prosaposin | P07602 |
| C0452138 | Sensorineural hearing loss, bilateral | PSAP | 5660 | prosaposin | P07602 |
| C0030567 | Parkinson Disease | PSAP | 5660 | prosaposin | P07602 |
| C1864651 | GAUCHER DISEASE, ATYPICAL, DUE TO SAPOSIN C DEFICIENCY | PSAP | 5660 | prosaposin | P07602 |
| C2673635 | Combined Saposin Deficiency | PSAP | 5660 | prosaposin | P07602 |
