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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 |
| Disease ID | Disease Name | Gene Symbol ▼ | Gene ID | Gene Name | UniProt ID |
|---|---|---|---|---|---|
| C0009595 | Obsessive-Compulsive Personality | COMT | 1312 | catechol-O-methyltransferase | P21964 |
| C3714756 | Intellectual Disability | COMT | 1312 | catechol-O-methyltransferase | P21964 |
| C0004930 | Behavior Disorders | COMT | 1312 | catechol-O-methyltransferase | P21964 |
| C0019294 | Hernia, Inguinal | COMT | 1312 | catechol-O-methyltransferase | P21964 |
| C0021051 | Immunologic Deficiency Syndromes | COMT | 1312 | catechol-O-methyltransferase | P21964 |
| C0027051 | Myocardial Infarction | COMT | 1312 | catechol-O-methyltransferase | P21964 |
| C0025958 | Microcephaly | COMT | 1312 | catechol-O-methyltransferase | P21964 |
| C0033578 | Prostatic Neoplasms | COMT | 1312 | catechol-O-methyltransferase | P21964 |
| C0029124 | Optic Atrophy | COMT | 1312 | catechol-O-methyltransferase | P21964 |
| C0009946 | Conversion disorder | COMT | 1312 | catechol-O-methyltransferase | P21964 |
| C0008297 | Choanal Atresia | COMT | 1312 | catechol-O-methyltransferase | P21964 |
| 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 |
