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 12326 - 12350 of 62743 in total
Disease ID Disease Name Gene Symbol ▲ Gene ID Gene Name UniProt ID
C0264408 Childhood asthma CHIA 27159 chitinase acidic Q9BZP6
C0003873 Rheumatoid Arthritis CHID1 66005 chitinase domain containing 1 Q9BWS9
C0008677 Bronchitis, Chronic CHID1 66005 chitinase domain containing 1 Q9BWS9
C0002066 Alkaptonuria CHIT1 1118 chitinase 1 Q13231
C0003850 Arteriosclerosis CHIT1 1118 chitinase 1 Q13231
C0028064 Niemann-Pick Diseases CHIT1 1118 chitinase 1 Q13231
C1961835 Gaucher Disease, Type 1 CHIT1 1118 chitinase 1 Q13231
C0264408 Childhood asthma CHIT1 1118 chitinase 1 Q13231
C0002736 Amyotrophic Lateral Sclerosis CHIT1 1118 chitinase 1 Q13231
C0220756 Niemann-Pick Disease, Type C CHIT1 1118 chitinase 1 Q13231
C0085131 Gangliosidosis GM1 CHIT1 1118 chitinase 1 Q13231
C0017205 Gaucher Disease CHIT1 1118 chitinase 1 Q13231
C0004096 Asthma CHIT1 1118 chitinase 1 Q13231
C0041296 Tuberculosis CHIT1 1118 chitinase 1 Q13231
C0151744 Myocardial Ischemia CHIT1 1118 chitinase 1 Q13231
C0005283 beta Thalassemia CHIT1 1118 chitinase 1 Q13231
C0010674 Cystic Fibrosis CHIT1 1118 chitinase 1 Q13231
C0022283 Incontinentia Pigmenti Achromians CHIT1 1118 chitinase 1 Q13231
C0243026 Sepsis CHIT1 1118 chitinase 1 Q13231
C0043208 Wolman Disease CHIT1 1118 chitinase 1 Q13231
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

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Last updated: August 19, 2024