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 61076 - 61100 of 62743 in total
Disease ID Disease Name Gene Symbol Gene ID Gene Name UniProt ID ▼
C0152105 Hypertensive heart disease SLC33A1 9197 solute carrier family 33 member 1 O00400
C1384514 Conn Syndrome SLC33A1 9197 solute carrier family 33 member 1 O00400
C0344315 Depressed mood SLC33A1 9197 solute carrier family 33 member 1 O00400
C0007222 Cardiovascular Diseases SLC33A1 9197 solute carrier family 33 member 1 O00400
C1510497 Lens Opacities SLC33A1 9197 solute carrier family 33 member 1 O00400
C0600139 Prostate carcinoma SLC33A1 9197 solute carrier family 33 member 1 O00400
C1561643 Chronic Kidney Diseases SLC33A1 9197 solute carrier family 33 member 1 O00400
C0027051 Myocardial Infarction SLC33A1 9197 solute carrier family 33 member 1 O00400
C0034152 Henoch-Schoenlein Purpura SLC33A1 9197 solute carrier family 33 member 1 O00400
C0524851 Neurodegenerative Disorders SLC33A1 9197 solute carrier family 33 member 1 O00400
C0020545 Hypertension, Renovascular SLC33A1 9197 solute carrier family 33 member 1 O00400
C0011847 Diabetes SLC33A1 9197 solute carrier family 33 member 1 O00400
C0017658 Glomerulonephritis SLC33A1 9197 solute carrier family 33 member 1 O00400
C0004238 Atrial Fibrillation SLC33A1 9197 solute carrier family 33 member 1 O00400
C0006826 Malignant Neoplasms SLC33A1 9197 solute carrier family 33 member 1 O00400
C1384666 hearing impairment SLC33A1 9197 solute carrier family 33 member 1 O00400
C0007786 Brain Ischemia SLC33A1 9197 solute carrier family 33 member 1 O00400
C0022658 Kidney Diseases SLC33A1 9197 solute carrier family 33 member 1 O00400
C0004153 Atherosclerosis SLC33A1 9197 solute carrier family 33 member 1 O00400
C1862941 Amyotrophic Lateral Sclerosis, Sporadic SLC33A1 9197 solute carrier family 33 member 1 O00400
C0796074 MOHR-TRANEBJAERG SYNDROME SLC33A1 9197 solute carrier family 33 member 1 O00400
C0007785 Cerebral Infarction SLC33A1 9197 solute carrier family 33 member 1 O00400
C4551858 Vesicoureteral Reflux 1 SLC33A1 9197 solute carrier family 33 member 1 O00400
C0376358 Malignant neoplasm of prostate SLC33A1 9197 solute carrier family 33 member 1 O00400
C0014547 Epilepsies, Partial SLC33A1 9197 solute carrier family 33 member 1 O00400

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Last updated: August 19, 2024