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 1926 - 1950 of 62743 in total
Disease ID Disease Name Gene Symbol Gene ID ▼ Gene Name UniProt ID
C0023434 Chronic Lymphocytic Leukemia COG1 9382 component of oligomeric golgi complex 1 Q8WTW3
C2931011 Congenital disorder of glycosylation, type 2G COG1 9382 component of oligomeric golgi complex 1 Q8WTW3
C0235946 Cerebral atrophy COG1 9382 component of oligomeric golgi complex 1 Q8WTW3
C0002871 Anemia COG1 9382 component of oligomeric golgi complex 1 Q8WTW3
C0265342 Cerebrocostomandibular Syndrome COG1 9382 component of oligomeric golgi complex 1 Q8WTW3
C0015934 Fetal Growth Retardation COG1 9382 component of oligomeric golgi complex 1 Q8WTW3
C0376545 Hematologic Neoplasms COG1 9382 component of oligomeric golgi complex 1 Q8WTW3
C0040034 Thrombocytopenia COG1 9382 component of oligomeric golgi complex 1 Q8WTW3
C0031900 Pierre Robin Syndrome COG1 9382 component of oligomeric golgi complex 1 Q8WTW3
C0575158 Kyphoscoliosis deformity of spine COG1 9382 component of oligomeric golgi complex 1 Q8WTW3
C0006413 Burkitt Lymphoma COG1 9382 component of oligomeric golgi complex 1 Q8WTW3
C1565489 Renal Insufficiency COG1 9382 component of oligomeric golgi complex 1 Q8WTW3
C0020295 Hydronephrosis COG1 9382 component of oligomeric golgi complex 1 Q8WTW3
C0848558 Hypospadias COG1 9382 component of oligomeric golgi complex 1 Q8WTW3
C0009081 Congenital clubfoot COG1 9382 component of oligomeric golgi complex 1 Q8WTW3
C1384666 hearing impairment COG1 9382 component of oligomeric golgi complex 1 Q8WTW3
C1842836 CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ii COG1 9382 component of oligomeric golgi complex 1 Q8WTW3
C3203102 Idiopathic pulmonary arterial hypertension COG1 9382 component of oligomeric golgi complex 1 Q8WTW3
C0036439 Scoliosis, unspecified COG1 9382 component of oligomeric golgi complex 1 Q8WTW3
C0268165 Primary hyperoxaluria type 2 GRHPR 9380 glyoxylate and hydroxypyruvate reductase Q9UBQ7
C0027709 Nephrocalcinosis GRHPR 9380 glyoxylate and hydroxypyruvate reductase Q9UBQ7
C0020501 Primary Hyperoxaluria GRHPR 9380 glyoxylate and hydroxypyruvate reductase Q9UBQ7
C0022650 Kidney Calculi GRHPR 9380 glyoxylate and hydroxypyruvate reductase Q9UBQ7
C0020500 Hyperoxaluria GRHPR 9380 glyoxylate and hydroxypyruvate reductase Q9UBQ7
C0392525 Nephrolithiasis GRHPR 9380 glyoxylate and hydroxypyruvate reductase Q9UBQ7

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Last updated: August 19, 2024