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 39376 - 39400 of 62743 in total
Disease ID Disease Name Gene Symbol Gene ID Gene Name ▲ UniProt ID
C0079773 Lymphoma, T-Cell, Cutaneous MBL2 4153 mannose binding lectin 2 P11226
C0041912 Upper Respiratory Infections MBL2 4153 mannose binding lectin 2 P11226
C0404521 Infective vaginitis MBL2 4153 mannose binding lectin 2 P11226
C0006267 Bronchiectasis MBL2 4153 mannose binding lectin 2 P11226
C0362046 Prediabetes syndrome MBL2 4153 mannose binding lectin 2 P11226
C0023240 Legionellosis MBL2 4153 mannose binding lectin 2 P11226
C2239176 Liver carcinoma MBL2 4153 mannose binding lectin 2 P11226
C0403414 Acute post-streptococcal glomerulonephritis MBL2 4153 mannose binding lectin 2 P11226
C0004364 Autoimmune Diseases MBL2 4153 mannose binding lectin 2 P11226
C0022408 Arthropathy MBL2 4153 mannose binding lectin 2 P11226
C0040136 Thyroid Neoplasm MBL2 4153 mannose binding lectin 2 P11226
C0011311 Dengue Fever MBL2 4153 mannose binding lectin 2 P11226
C0041321 Tuberculosis, Miliary MBL2 4153 mannose binding lectin 2 P11226
C0013537 Eclampsia MBL2 4153 mannose binding lectin 2 P11226
C0024198 Lyme Disease MBL2 4153 mannose binding lectin 2 P11226
C0677607 Hashimoto Disease MBL2 4153 mannose binding lectin 2 P11226
C0339789 Congenital deafness MBL2 4153 mannose binding lectin 2 P11226
C0026850 Muscular Dystrophy MBL2 4153 mannose binding lectin 2 P11226
C0028754 Obesity MBL2 4153 mannose binding lectin 2 P11226
C0409974 Lupus Erythematosus MBL2 4153 mannose binding lectin 2 P11226
C0399352 Developmental absence of tooth MBL2 4153 mannose binding lectin 2 P11226
C0003850 Arteriosclerosis MBL2 4153 mannose binding lectin 2 P11226
C0155626 Acute myocardial infarction MBL2 4153 mannose binding lectin 2 P11226
C0085436 Meningitis, Cryptococcal MBL2 4153 mannose binding lectin 2 P11226
C0162539 IgG Deficiency disorder MBL2 4153 mannose binding lectin 2 P11226

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Last updated: August 19, 2024