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 |
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DisGeNET | July 29, 2024 |
Disease ID | Disease Name | Gene Symbol ▲ | Gene ID | Gene Name | UniProt ID |
---|---|---|---|---|---|
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 |
C0011860 | Diabetes Mellitus, Non-Insulin-Dependent | COG2 | 22796 | component of oligomeric golgi complex 2 | Q14746 |
C0004238 | Atrial Fibrillation | COG2 | 22796 | component of oligomeric golgi complex 2 | Q14746 |
C0009806 | Constipation | COG2 | 22796 | component of oligomeric golgi complex 2 | Q14746 |
C0036572 | Seizures | COG2 | 22796 | component of oligomeric golgi complex 2 | Q14746 |
C0020445 | Hypercholesterolemia, Familial | COG2 | 22796 | component of oligomeric golgi complex 2 | Q14746 |
C4479353 | CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIq | COG2 | 22796 | component of oligomeric golgi complex 2 | Q14746 |
C0020597 | Hypobetalipoproteinemias | COG2 | 22796 | component of oligomeric golgi complex 2 | Q14746 |
C0745103 | Hyperlipoproteinemia Type IIa | COG2 | 22796 | component of oligomeric golgi complex 2 | Q14746 |
C1956346 | Coronary Artery Disease | COG2 | 22796 | component of oligomeric golgi complex 2 | Q14746 |
C0699791 | Stomach Carcinoma | COG2 | 22796 | component of oligomeric golgi complex 2 | Q14746 |
C0003873 | Rheumatoid Arthritis | COG2 | 22796 | component of oligomeric golgi complex 2 | Q14746 |
C0282577 | Congenital Disorders of Glycosylation | COG2 | 22796 | component of oligomeric golgi complex 2 | Q14746 |
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Last updated: August 19, 2024