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 |
---|---|---|---|---|---|
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 |
C1378703 | Renal carcinoma | COMT | 1312 | catechol-O-methyltransferase | P21964 |
C0003850 | Arteriosclerosis | COMT | 1312 | catechol-O-methyltransferase | P21964 |
C1838244 | TIBIAL MUSCULAR DYSTROPHY, TARDIVE | COMT | 1312 | catechol-O-methyltransferase | P21964 |
C4552000 | Episodic Kinesigenic Dyskinesia 1 | COMT | 1312 | catechol-O-methyltransferase | P21964 |
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Last updated: August 19, 2024