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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 |
|---|---|---|---|---|---|
| C0236663 | Alcohol withdrawal syndrome | COMT | 1312 | catechol-O-methyltransferase | P21964 |
| C0036337 | Schizoaffective Disorder | COMT | 1312 | catechol-O-methyltransferase | P21964 |
| C0040034 | Thrombocytopenia | COMT | 1312 | catechol-O-methyltransferase | P21964 |
| C1257931 | Mammary Neoplasms, Human | COMT | 1312 | catechol-O-methyltransferase | P21964 |
| C0349231 | Phobic anxiety disorder | COMT | 1312 | catechol-O-methyltransferase | P21964 |
| C0023492 | Leukemia, T-Cell | COMT | 1312 | catechol-O-methyltransferase | P21964 |
| C4048328 | cervical cancer | COMT | 1312 | catechol-O-methyltransferase | P21964 |
| C0279626 | Squamous cell carcinoma of esophagus | COMT | 1312 | catechol-O-methyltransferase | P21964 |
| C0027819 | Neuroblastoma | COMT | 1312 | catechol-O-methyltransferase | P21964 |
| C0013336 | Dwarfism | COMT | 1312 | catechol-O-methyltransferase | P21964 |
| C0008350 | Cholelithiasis | COMT | 1312 | catechol-O-methyltransferase | P21964 |
| C0476254 | Dyslexia | COMT | 1312 | catechol-O-methyltransferase | P21964 |
| C0028043 | Nicotine Dependence | COMT | 1312 | catechol-O-methyltransferase | P21964 |
| C0032460 | Polycystic Ovary Syndrome | COMT | 1312 | catechol-O-methyltransferase | P21964 |
| C0007102 | Malignant tumor of colon | COMT | 1312 | catechol-O-methyltransferase | P21964 |
| C1956346 | Coronary Artery Disease | COMT | 1312 | catechol-O-methyltransferase | P21964 |
| C0010068 | Coronary heart disease | COMT | 1312 | catechol-O-methyltransferase | P21964 |
| C1510586 | Autism Spectrum Disorders | COMT | 1312 | catechol-O-methyltransferase | P21964 |
| C0009081 | Congenital clubfoot | COMT | 1312 | catechol-O-methyltransferase | P21964 |
| C0030044 | Acrocephaly | COMT | 1312 | catechol-O-methyltransferase | P21964 |
| C0004352 | Autistic Disorder | COMT | 1312 | catechol-O-methyltransferase | P21964 |
| C0003864 | Arthritis | COMT | 1312 | catechol-O-methyltransferase | P21964 |
| C0040332 | Tobacco Dependence | COMT | 1312 | catechol-O-methyltransferase | P21964 |
| C0848558 | Hypospadias | COMT | 1312 | catechol-O-methyltransferase | P21964 |
| C0013080 | Down Syndrome | COMT | 1312 | catechol-O-methyltransferase | P21964 |
