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 59176 - 59200 of 62743 in total
Disease ID Disease Name Gene Symbol Gene ID ▼ Gene Name UniProt ID
C0278510 Childhood Medulloblastoma TREH 11181 trehalase O43280
C0338508 Optic Atrophy 1 TREH 11181 trehalase O43280
C0019348 Herpes Simplex Infections TREH 11181 trehalase O43280
C0278876 Adult Medulloblastoma TREH 11181 trehalase O43280
C0006826 Malignant Neoplasms TREH 11181 trehalase O43280
C0011860 Diabetes Mellitus, Non-Insulin-Dependent TREH 11181 trehalase O43280
C0400966 Non-alcoholic Fatty Liver Disease TREH 11181 trehalase O43280
C0278878 Adult Glioblastoma TREH 11181 trehalase O43280
C0003873 Rheumatoid Arthritis TREH 11181 trehalase O43280
C0011849 Diabetes Mellitus TREH 11181 trehalase O43280
C0027651 Neoplasms TREH 11181 trehalase O43280
C2239176 Liver carcinoma TREH 11181 trehalase O43280
C0022658 Kidney Diseases TREH 11181 trehalase O43280
C0087012 Ataxia, Spinocerebellar TREH 11181 trehalase O43280
C0037930 Spinal Cord Neoplasms TREH 11181 trehalase O43280
C0011991 Diarrhea TREH 11181 trehalase O43280
C0684249 Carcinoma of lung TREH 11181 trehalase O43280
C1306459 Primary malignant neoplasm TREH 11181 trehalase O43280
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

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Last updated: August 19, 2024