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 50401 - 50425 of 62743 in total
Disease ID Disease Name Gene Symbol ▼ Gene ID Gene Name UniProt ID
C0162309 Adrenoleukodystrophy CHIT1 1118 chitinase 1 Q13231
C0032463 Polycythemia Vera CHIT1 1118 chitinase 1 Q13231
C1292778 Chronic myeloproliferative disorder CHIT1 1118 chitinase 1 Q13231
C0002895 Anemia, Sickle Cell CHIT1 1118 chitinase 1 Q13231
C0442874 Neuropathy CHIT1 1118 chitinase 1 Q13231
C3495559 Juvenile arthritis CHIT1 1118 chitinase 1 Q13231
C1956346 Coronary Artery Disease CHIT1 1118 chitinase 1 Q13231
C0400966 Non-alcoholic Fatty Liver Disease CHIT1 1118 chitinase 1 Q13231
C0007282 Carotid Stenosis CHIT1 1118 chitinase 1 Q13231
C0024115 Lung diseases CHIT1 1118 chitinase 1 Q13231
C0010054 Coronary Arteriosclerosis CHIT1 1118 chitinase 1 Q13231
C0020474 Hyperlipidemia, Familial Combined CHIT1 1118 chitinase 1 Q13231
C0011269 Dementia, Vascular CHIT1 1118 chitinase 1 Q13231
C3888317 Sialidosis, type 2 CHIT1 1118 chitinase 1 Q13231
C0338451 Frontotemporal dementia CHIT1 1118 chitinase 1 Q13231
C0003873 Rheumatoid Arthritis CHID1 66005 chitinase domain containing 1 Q9BWS9
C0008677 Bronchitis, Chronic CHID1 66005 chitinase domain containing 1 Q9BWS9
C0004096 Asthma CHIA 27159 chitinase acidic Q9BZP6
C0022577 Keratoconjunctivitis, Vernal CHIA 27159 chitinase acidic Q9BZP6
C0155877 Allergic asthma CHIA 27159 chitinase acidic Q9BZP6
C0341106 Eosinophilic esophagitis CHIA 27159 chitinase acidic Q9BZP6
C1527336 Sjogren's Syndrome CHIA 27159 chitinase acidic Q9BZP6
C0013238 Dry Eye Syndromes CHIA 27159 chitinase acidic Q9BZP6
C2607914 Allergic rhinitis (disorder) CHIA 27159 chitinase acidic Q9BZP6
C0264408 Childhood asthma CHIA 27159 chitinase acidic Q9BZP6

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Last updated: August 19, 2024