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 |
---|---|---|---|---|---|
C0520680 | Sleep Apnea, Central | COMT | 1312 | catechol-O-methyltransferase | P21964 |
C0009806 | Constipation | COMT | 1312 | catechol-O-methyltransferase | P21964 |
C0432215 | Progressive pseudorheumatoid dysplasia | COMT | 1312 | catechol-O-methyltransferase | P21964 |
C0029421 | Osteochondritis Dissecans | COMT | 1312 | catechol-O-methyltransferase | P21964 |
C0600139 | Prostate carcinoma | COMT | 1312 | catechol-O-methyltransferase | P21964 |
C0026010 | Microphthalmos | COMT | 1312 | catechol-O-methyltransferase | P21964 |
C0027404 | Narcolepsy | COMT | 1312 | catechol-O-methyltransferase | P21964 |
C0042580 | Vesico-Ureteral Reflux | COMT | 1312 | catechol-O-methyltransferase | P21964 |
C0011206 | Delirium | COMT | 1312 | catechol-O-methyltransferase | P21964 |
C0002895 | Anemia, Sickle Cell | COMT | 1312 | catechol-O-methyltransferase | P21964 |
C0003125 | Anorexia Nervosa | COMT | 1312 | catechol-O-methyltransferase | P21964 |
C0029227 | Delirium, Dementia, Amnestic, Cognitive Disorders | COMT | 1312 | catechol-O-methyltransferase | P21964 |
C0007134 | Renal Cell Carcinoma | COMT | 1312 | catechol-O-methyltransferase | P21964 |
C0038454 | Cerebrovascular accident | COMT | 1312 | catechol-O-methyltransferase | P21964 |
C1332206 | Adult Lymphoma | COMT | 1312 | catechol-O-methyltransferase | P21964 |
C0700613 | Anxiety state | COMT | 1312 | catechol-O-methyltransferase | P21964 |
C0524851 | Neurodegenerative Disorders | COMT | 1312 | catechol-O-methyltransferase | P21964 |
C0015934 | Fetal Growth Retardation | COMT | 1312 | catechol-O-methyltransferase | P21964 |
C0699885 | Carcinoma of bladder | COMT | 1312 | catechol-O-methyltransferase | P21964 |
C0027765 | nervous system disorder | COMT | 1312 | catechol-O-methyltransferase | P21964 |
C0149654 | Conduct Disorder | COMT | 1312 | catechol-O-methyltransferase | P21964 |
C0031212 | Personality Disorders | COMT | 1312 | catechol-O-methyltransferase | P21964 |
C0699791 | Stomach Carcinoma | COMT | 1312 | catechol-O-methyltransferase | P21964 |
C0431375 | Classical Lissencephaly | COMT | 1312 | catechol-O-methyltransferase | P21964 |
C0853193 | Bipolar I disorder | COMT | 1312 | catechol-O-methyltransferase | P21964 |
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