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 61101 - 61125 of 62743 in total
Disease ID Disease Name Gene Symbol Gene ID Gene Name UniProt ID ▼
C0155616 Secondary hypertension SLC33A1 9197 solute carrier family 33 member 1 O00400
C1956346 Coronary Artery Disease SLC33A1 9197 solute carrier family 33 member 1 O00400
C0002395 Alzheimer's Disease SLC33A1 9197 solute carrier family 33 member 1 O00400
C0086543 Cataract SLC33A1 9197 solute carrier family 33 member 1 O00400
C0038454 Cerebrovascular accident SLC33A1 9197 solute carrier family 33 member 1 O00400
C0007194 Hypertrophic Cardiomyopathy SLC33A1 9197 solute carrier family 33 member 1 O00400
C0024796 Marfan Syndrome SLC33A1 9197 solute carrier family 33 member 1 O00400
C0206624 Hepatoblastoma SLC33A1 9197 solute carrier family 33 member 1 O00400
C0011581 Depressive disorder SLC33A1 9197 solute carrier family 33 member 1 O00400
C0001430 Adenoma SLC33A1 9197 solute carrier family 33 member 1 O00400
C0037772 Spastic Paraplegia SLC33A1 9197 solute carrier family 33 member 1 O00400
C0010054 Coronary Arteriosclerosis SLC33A1 9197 solute carrier family 33 member 1 O00400
C0524524 Pseudoaphakia SLC33A1 9197 solute carrier family 33 member 1 O00400
C1510586 Autism Spectrum Disorders SLC33A1 9197 solute carrier family 33 member 1 O00400
C0011860 Diabetes Mellitus, Non-Insulin-Dependent SLC33A1 9197 solute carrier family 33 member 1 O00400
C0235946 Cerebral atrophy SLC33A1 9197 solute carrier family 33 member 1 O00400
C0003811 Cardiac Arrhythmia SLC33A1 9197 solute carrier family 33 member 1 O00400
C0162871 Aortic Aneurysm, Abdominal SLC33A1 9197 solute carrier family 33 member 1 O00400
C1704272 Benign Prostatic Hyperplasia SLC33A1 9197 solute carrier family 33 member 1 O00400
C0009402 Colorectal Carcinoma SLC33A1 9197 solute carrier family 33 member 1 O00400
C0151744 Myocardial Ischemia SLC33A1 9197 solute carrier family 33 member 1 O00400
C0036421 Systemic Scleroderma SLC33A1 9197 solute carrier family 33 member 1 O00400
C0030567 Parkinson Disease SLC33A1 9197 solute carrier family 33 member 1 O00400
C0014175 Endometriosis SLC33A1 9197 solute carrier family 33 member 1 O00400
C0010068 Coronary heart disease SLC33A1 9197 solute carrier family 33 member 1 O00400

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Last updated: August 19, 2024