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
Displaying entries 12976 - 13000 of 62743 in total
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