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 |
---|---|---|---|---|---|
C0854723 | Retinal Dystrophies | PRPS1 | 5631 | phosphoribosyl pyrophosphate synthetase 1 | P60891 |
C0751606 | Adult Acute Lymphocytic Leukemia | PRPS1 | 5631 | phosphoribosyl pyrophosphate synthetase 1 | P60891 |
C0151313 | Sensory neuropathy | PRPS1 | 5631 | phosphoribosyl pyrophosphate synthetase 1 | P60891 |
C0009402 | Colorectal Carcinoma | PRPS1 | 5631 | phosphoribosyl pyrophosphate synthetase 1 | P60891 |
C0023449 | Acute lymphocytic leukemia | PRPS1 | 5631 | phosphoribosyl pyrophosphate synthetase 1 | P60891 |
C3714756 | Intellectual Disability | PRPS1 | 5631 | phosphoribosyl pyrophosphate synthetase 1 | P60891 |
C0017636 | Glioblastoma | PRPS1 | 5631 | phosphoribosyl pyrophosphate synthetase 1 | P60891 |
C0031117 | Peripheral Neuropathy | PRPS1 | 5631 | phosphoribosyl pyrophosphate synthetase 1 | P60891 |
C0027819 | Neuroblastoma | PRPS1 | 5631 | phosphoribosyl pyrophosphate synthetase 1 | P60891 |
C3887709 | Optic Neuropathy | PRPS1 | 5631 | phosphoribosyl pyrophosphate synthetase 1 | P60891 |
C0392553 | Hereditary peripheral neuropathy | PRPS1 | 5631 | phosphoribosyl pyrophosphate synthetase 1 | P60891 |
C0442874 | Neuropathy | PRPS1 | 5631 | phosphoribosyl pyrophosphate synthetase 1 | P60891 |
C0028738 | Nystagmus | PRPS1 | 5631 | phosphoribosyl pyrophosphate synthetase 1 | P60891 |
C3665347 | Visual Impairment | PRPS1 | 5631 | phosphoribosyl pyrophosphate synthetase 1 | P60891 |
C0023015 | Language Disorders | PRPS1 | 5631 | phosphoribosyl pyrophosphate synthetase 1 | P60891 |
C0678222 | Breast Carcinoma | PRPS1 | 5631 | phosphoribosyl pyrophosphate synthetase 1 | P60891 |
C0162429 | Malnutrition | PRPS1 | 5631 | phosphoribosyl pyrophosphate synthetase 1 | P60891 |
C0034372 | Quadriplegia | PRPS1 | 5631 | phosphoribosyl pyrophosphate synthetase 1 | P60891 |
C0403719 | Uric acid urolithiasis | PRPS1 | 5631 | phosphoribosyl pyrophosphate synthetase 1 | P60891 |
C0013336 | Dwarfism | PRPS1 | 5631 | phosphoribosyl pyrophosphate synthetase 1 | P60891 |
C0004114 | Astrocytoma | PRPS1 | 5631 | phosphoribosyl pyrophosphate synthetase 1 | P60891 |
C1565489 | Renal Insufficiency | PRPS1 | 5631 | phosphoribosyl pyrophosphate synthetase 1 | P60891 |
C0524851 | Neurodegenerative Disorders | PRNP | 5621 | prion protein | P04156 |
C1852467 | Creutzfeldt-Jakob Disease, Sporadic | PRNP | 5621 | prion protein | P04156 |
C0162534 | Prion Diseases | PRNP | 5621 | prion protein | P04156 |
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Last updated: August 19, 2024