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 14501 - 14525 of 62743 in total
Disease ID Disease Name Gene Symbol ▼ Gene ID Gene Name UniProt ID
C0025202 melanoma PNP 4860 purine nucleoside phosphorylase P00491
C0042373 Vascular Diseases PNP 4860 purine nucleoside phosphorylase P00491
C0162671 MELAS Syndrome PNP 4860 purine nucleoside phosphorylase P00491
C1970827 Phosphoribosylpyrophosphate Synthetase Superactivity PNP 4860 purine nucleoside phosphorylase P00491
C1961102 Precursor Cell Lymphoblastic Leukemia Lymphoma PNP 4860 purine nucleoside phosphorylase P00491
C2700553 Omenn Syndrome PNP 4860 purine nucleoside phosphorylase P00491
C1332979 Childhood Lymphoma PNP 4860 purine nucleoside phosphorylase P00491
C0238051 Cerebral Angiitis PNP 4860 purine nucleoside phosphorylase P00491
C0031090 Periodontal Diseases PNP 4860 purine nucleoside phosphorylase P00491
C0024312 Lymphopenia PNP 4860 purine nucleoside phosphorylase P00491
C0005684 Malignant neoplasm of urinary bladder PNP 4860 purine nucleoside phosphorylase P00491
C0086438 Hypogammaglobulinemia PNP 4860 purine nucleoside phosphorylase P00491
C0021053 Immune System Diseases PNP 4860 purine nucleoside phosphorylase P00491
C0494261 Combined immunodeficiency PNP 4860 purine nucleoside phosphorylase P00491
C0041296 Tuberculosis PNP 4860 purine nucleoside phosphorylase P00491
C0007097 Carcinoma PNP 4860 purine nucleoside phosphorylase P00491
C3714756 Intellectual Disability PNP 4860 purine nucleoside phosphorylase P00491
C0031099 Periodontitis PNP 4860 purine nucleoside phosphorylase P00491
C1334647 Maxillary Sinus Squamous Cell Carcinoma PNP 4860 purine nucleoside phosphorylase P00491
C0003850 Arteriosclerosis PNP 4860 purine nucleoside phosphorylase P00491
C0029456 Osteoporosis PNP 4860 purine nucleoside phosphorylase P00491
C0021051 Immunologic Deficiency Syndromes PNP 4860 purine nucleoside phosphorylase P00491
C0268119 Combined molybdoflavoprotein enzyme deficiency PNP 4860 purine nucleoside phosphorylase P00491
C0546837 Malignant neoplasm of esophagus PNP 4860 purine nucleoside phosphorylase P00491
C0006142 Malignant neoplasm of breast PNP 4860 purine nucleoside phosphorylase P00491

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Last updated: August 19, 2024