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 50376 - 50400 of 62743 in total
Disease ID Disease Name Gene Symbol ▼ Gene ID Gene Name UniProt ID
C0268251 Gaucher Disease, Type 3 (disorder) CHIT1 1118 chitinase 1 Q13231
C0268242 Niemann-Pick Disease, Type A CHIT1 1118 chitinase 1 Q13231
C2607914 Allergic rhinitis (disorder) CHIT1 1118 chitinase 1 Q13231
C0206062 Lung Diseases, Interstitial CHIT1 1118 chitinase 1 Q13231
C0011847 Diabetes CHIT1 1118 chitinase 1 Q13231
C0010068 Coronary heart disease CHIT1 1118 chitinase 1 Q13231
C0155877 Allergic asthma CHIT1 1118 chitinase 1 Q13231
C2350621 Eumycetoma CHIT1 1118 chitinase 1 Q13231
C1096903 Sialic Acid Storage Disease, Finnish Type (disorder) CHIT1 1118 chitinase 1 Q13231
C0221056 Adult type dermatomyositis CHIT1 1118 chitinase 1 Q13231
C0027022 Myeloproliferative disease CHIT1 1118 chitinase 1 Q13231
C0678222 Breast Carcinoma CHIT1 1118 chitinase 1 Q13231
C0022658 Kidney Diseases CHIT1 1118 chitinase 1 Q13231
C0006142 Malignant neoplasm of breast CHIT1 1118 chitinase 1 Q13231
C0010414 Infection by Cryptococcus neoformans CHIT1 1118 chitinase 1 Q13231
C0031069 Familial Mediterranean Fever CHIT1 1118 chitinase 1 Q13231
C0019196 Hepatitis C CHIT1 1118 chitinase 1 Q13231
C2937421 Prostatic Hyperplasia CHIT1 1118 chitinase 1 Q13231
C0239946 Fibrosis, Liver CHIT1 1118 chitinase 1 Q13231
C1285162 Degenerative disorder CHIT1 1118 chitinase 1 Q13231
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

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Last updated: August 19, 2024