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 |
Disease ID | Disease Name | Gene Symbol ▲ | Gene ID | Gene Name | UniProt ID |
---|---|---|---|---|---|
C0022336 | Creutzfeldt-Jakob disease | CHIT1 | 1118 | chitinase 1 | Q13231 |
C0033578 | Prostatic Neoplasms | CHIT1 | 1118 | chitinase 1 | Q13231 |
C0011860 | Diabetes Mellitus, Non-Insulin-Dependent | CHIT1 | 1118 | chitinase 1 | Q13231 |
C0024530 | Malaria | CHIT1 | 1118 | chitinase 1 | Q13231 |
C0024301 | Lymphoma, Follicular | CHIT1 | 1118 | chitinase 1 | Q13231 |
C0268250 | Gaucher Disease, Type 2 (disorder) | CHIT1 | 1118 | chitinase 1 | Q13231 |
C0026697 | Mucolipidoses | CHIT1 | 1118 | chitinase 1 | Q13231 |
C0009402 | Colorectal Carcinoma | CHIT1 | 1118 | chitinase 1 | Q13231 |
C0342853 | Sialuria | CHIT1 | 1118 | chitinase 1 | Q13231 |
C0085078 | Lysosomal Storage Diseases | CHIT1 | 1118 | chitinase 1 | Q13231 |
C0268226 | Type I Mucolipidosis | CHIT1 | 1118 | chitinase 1 | Q13231 |
C0006826 | Malignant Neoplasms | CHIT1 | 1118 | chitinase 1 | Q13231 |
C2936664 | Acquired Hypogammaglobulinemia | CHIT1 | 1118 | chitinase 1 | Q13231 |
C0026769 | Multiple Sclerosis | CHIT1 | 1118 | chitinase 1 | Q13231 |
C0023467 | Leukemia, Myelocytic, Acute | CHIT1 | 1118 | chitinase 1 | Q13231 |
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 |
GlyCosmos is a member of the GlySpace Alliance together with GlyGen and Glycomics@ExPASy.
Supported by JST NBDC Grant Number JPMJND2204
Partly supported by NIH Common Fund Grant #1U01GM125267-01
GlyCosmos Portal v4.0.0
Last updated: August 19, 2024