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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
Displaying entries 57651 - 57675 of 62743 in total
Disease ID Disease Name Gene Symbol Gene ID Gene Name UniProt ID ▼
C0085859 Polyglandular Type I Autoimmune Syndrome FCGR3B 2215 Fc fragment of IgG receptor IIIb O75015
C0027051 Myocardial Infarction FCGR3B 2215 Fc fragment of IgG receptor IIIb O75015
C0010414 Infection by Cryptococcus neoformans FCGR3B 2215 Fc fragment of IgG receptor IIIb O75015
C0025202 melanoma FCGR3B 2215 Fc fragment of IgG receptor IIIb O75015
C0023493 Adult T-Cell Lymphoma/Leukemia FCGR3B 2215 Fc fragment of IgG receptor IIIb O75015
C0007097 Carcinoma FCGR3B 2215 Fc fragment of IgG receptor IIIb O75015
C0001339 Acute pancreatitis FCGR3B 2215 Fc fragment of IgG receptor IIIb O75015
C0400966 Non-alcoholic Fatty Liver Disease FCGR3B 2215 Fc fragment of IgG receptor IIIb O75015
C0019189 Hepatitis, Chronic FCGR3B 2215 Fc fragment of IgG receptor IIIb O75015
C1855520 Hyperglycemia, Postprandial FCGR3B 2215 Fc fragment of IgG receptor IIIb O75015
C1704321 Nephrotic Syndrome, Minimal Change FCGR3B 2215 Fc fragment of IgG receptor IIIb O75015
C1168401 Squamous cell carcinoma of the head and neck FCGR3B 2215 Fc fragment of IgG receptor IIIb O75015
C0014175 Endometriosis FCGR3B 2215 Fc fragment of IgG receptor IIIb O75015
C2931187 Nephropathic cystinosis CTNS 1497 cystinosin, lysosomal cystine transporter O60931
C4316899 Cystinosis CTNS 1497 cystinosin, lysosomal cystine transporter O60931
C0268626 Juvenile nephropathic cystinosis (disorder) CTNS 1497 cystinosin, lysosomal cystine transporter O60931
C0015624 Fanconi Syndrome CTNS 1497 cystinosin, lysosomal cystine transporter O60931
C2931013 Cystinosis, benign, nonnephropathic CTNS 1497 cystinosin, lysosomal cystine transporter O60931
C0235946 Cerebral atrophy CTNS 1497 cystinosin, lysosomal cystine transporter O60931
C0085078 Lysosomal Storage Diseases CTNS 1497 cystinosin, lysosomal cystine transporter O60931
C0030567 Parkinson Disease CTNS 1497 cystinosin, lysosomal cystine transporter O60931
C0341703 Adult Fanconi syndrome CTNS 1497 cystinosin, lysosomal cystine transporter O60931
C1565489 Renal Insufficiency CTNS 1497 cystinosin, lysosomal cystine transporter O60931
C0022658 Kidney Diseases CTNS 1497 cystinosin, lysosomal cystine transporter O60931
C2749685 CYSTINOSIS, ATYPICAL NEPHROPATHIC (disorder) CTNS 1497 cystinosin, lysosomal cystine transporter O60931
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Last updated: August 19, 2024