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 45401 - 45425 of 62743 in total
Disease ID Disease Name Gene Symbol Gene ID Gene Name UniProt ID ▲
C0004153 Atherosclerosis CHIT1 1118 chitinase 1 Q13231
C0009447 Common Variable Immunodeficiency CHIT1 1118 chitinase 1 Q13231
C0002395 Alzheimer's Disease CHIT1 1118 chitinase 1 Q13231
C0040028 Thrombocythemia, Essential CHIT1 1118 chitinase 1 Q13231
C0027583 Nematode infections CHIT1 1118 chitinase 1 Q13231
C0948008 Ischemic stroke CHIT1 1118 chitinase 1 Q13231
C0024449 Mycetoma CHIT1 1118 chitinase 1 Q13231
C0023794 Lipoidosis CHIT1 1118 chitinase 1 Q13231
C1306459 Primary malignant neoplasm CHIT1 1118 chitinase 1 Q13231
C0024117 Chronic Obstructive Airway Disease CHIT1 1118 chitinase 1 Q13231
C0017152 Gastritis CHIT1 1118 chitinase 1 Q13231
C0524851 Neurodegenerative Disorders CHIT1 1118 chitinase 1 Q13231
C0855139 Monocytoid B-cell lymphoma CHIT1 1118 chitinase 1 Q13231
C0497327 Dementia CHIT1 1118 chitinase 1 Q13231
C0036202 Sarcoidosis CHIT1 1118 chitinase 1 Q13231
C0520679 Sleep Apnea, Obstructive CHIT1 1118 chitinase 1 Q13231
C0023521 Globoid cell leukodystrophy CHIT1 1118 chitinase 1 Q13231
C0002726 Amyloidosis CHIT1 1118 chitinase 1 Q13231
C0016085 Filariasis CHIT1 1118 chitinase 1 Q13231
C2711227 Steatohepatitis CHIT1 1118 chitinase 1 Q13231
C0011265 Presenile dementia CHIT1 1118 chitinase 1 Q13231
C0034069 Pulmonary Fibrosis CHIT1 1118 chitinase 1 Q13231
C0002875 Cooley's anemia CHIT1 1118 chitinase 1 Q13231
C0021832 Intestinal Diseases, Parasitic CHIT1 1118 chitinase 1 Q13231
C0030567 Parkinson Disease CHIT1 1118 chitinase 1 Q13231

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Last updated: August 19, 2024