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 |
---|---|---|---|---|---|
C0020676 | Hypothyroidism | COMT | 1312 | catechol-O-methyltransferase | P21964 |
C0085109 | Corneal Neovascularization | COMT | 1312 | catechol-O-methyltransferase | P21964 |
C1862389 | ATRIAL SEPTAL DEFECT 1 | COMT | 1312 | catechol-O-methyltransferase | P21964 |
C0036349 | Paranoid Schizophrenia | COMT | 1312 | catechol-O-methyltransferase | P21964 |
C0012734 | Disruptive Behavior Disorder | COMT | 1312 | catechol-O-methyltransferase | P21964 |
C0699790 | Colon Carcinoma | COMT | 1312 | catechol-O-methyltransferase | P21964 |
C0338480 | Common Migraine | COMT | 1312 | catechol-O-methyltransferase | P21964 |
C0036572 | Seizures | COMT | 1312 | catechol-O-methyltransferase | P21964 |
C0025322 | Premature Menopause | COMT | 1312 | catechol-O-methyltransferase | P21964 |
C0002902 | Anencephaly | COMT | 1312 | catechol-O-methyltransferase | P21964 |
C0432306 | Ichthyosis Bullosa of Siemens | COMT | 1312 | catechol-O-methyltransferase | P21964 |
C0007847 | Malignant tumor of cervix | COMT | 1312 | catechol-O-methyltransferase | P21964 |
C0271441 | Chronic otitis media | COMT | 1312 | catechol-O-methyltransferase | P21964 |
C1561643 | Chronic Kidney Diseases | COMT | 1312 | catechol-O-methyltransferase | P21964 |
C0033937 | Psychoses, Drug | COMT | 1312 | catechol-O-methyltransferase | P21964 |
C4552100 | Lynch Syndrome | COMT | 1312 | catechol-O-methyltransferase | P21964 |
C0086543 | Cataract | COMT | 1312 | catechol-O-methyltransferase | P21964 |
C0017601 | Glaucoma | COMT | 1312 | catechol-O-methyltransferase | P21964 |
C0036439 | Scoliosis, unspecified | COMT | 1312 | catechol-O-methyltransferase | P21964 |
C0039496 | Temporomandibular Joint Dysfunction Syndrome | COMT | 1312 | catechol-O-methyltransferase | P21964 |
C0021122 | Disruptive, Impulse Control, and Conduct Disorders | COMT | 1312 | catechol-O-methyltransferase | P21964 |
C0014170 | Endometrial Neoplasms | COMT | 1312 | catechol-O-methyltransferase | P21964 |
C0752347 | Lewy Body Disease | COMT | 1312 | catechol-O-methyltransferase | P21964 |
C0010417 | Cryptorchidism | COMT | 1312 | catechol-O-methyltransferase | P21964 |
C0036939 | Shared Paranoid 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