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 59276 - 59300 of 62743 in total
Disease ID Disease Name Gene Symbol Gene ID ▼ Gene Name UniProt ID
C0001815 Primary Myelofibrosis CHIT1 1118 chitinase 1 Q13231
C0029410 Osteoarthritis of hip CHIT1 1118 chitinase 1 Q13231
C0268243 Niemann-Pick Disease, Type B CHIT1 1118 chitinase 1 Q13231
C0008370 Cholestasis CHIT1 1118 chitinase 1 Q13231
C0026987 Myelofibrosis CHIT1 1118 chitinase 1 Q13231
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
C0002736 Amyotrophic Lateral Sclerosis CHI3L2 1117 chitinase 3 like 2 Q15782
C0029408 Degenerative polyarthritis CHI3L2 1117 chitinase 3 like 2 Q15782
C0006142 Malignant neoplasm of breast CHI3L2 1117 chitinase 3 like 2 Q15782
C0007134 Renal Cell Carcinoma CHI3L2 1117 chitinase 3 like 2 Q15782
C0027651 Neoplasms CHI3L2 1117 chitinase 3 like 2 Q15782

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Last updated: August 19, 2024