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 |
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DisGeNET | July 29, 2024 |
Disease ID | Disease Name | Gene Symbol | Gene ID | Gene Name | UniProt ID ▲ |
---|---|---|---|---|---|
C0015397 | Disorder of eye | CYP27A1 | 1593 | cytochrome P450 family 27 subfamily A member 1 | Q02318 |
C1510586 | Autism Spectrum Disorders | CYP27A1 | 1593 | cytochrome P450 family 27 subfamily A member 1 | Q02318 |
C0235946 | Cerebral atrophy | CYP27A1 | 1593 | cytochrome P450 family 27 subfamily A member 1 | Q02318 |
C0268689 | Vitamin D-dependent rickets, type 1 | CYP27A1 | 1593 | cytochrome P450 family 27 subfamily A member 1 | Q02318 |
C0239946 | Fibrosis, Liver | CYP27A1 | 1593 | cytochrome P450 family 27 subfamily A member 1 | Q02318 |
C0497327 | Dementia | CYP27A1 | 1593 | cytochrome P450 family 27 subfamily A member 1 | Q02318 |
C0005684 | Malignant neoplasm of urinary bladder | CYP27A1 | 1593 | cytochrome P450 family 27 subfamily A member 1 | Q02318 |
C0011991 | Diarrhea | CYP27A1 | 1593 | cytochrome P450 family 27 subfamily A member 1 | Q02318 |
C0013595 | Eczema | CYP27A1 | 1593 | cytochrome P450 family 27 subfamily A member 1 | Q02318 |
C0027051 | Myocardial Infarction | CYP27A1 | 1593 | cytochrome P450 family 27 subfamily A member 1 | Q02318 |
C0153452 | Malignant neoplasm of gallbladder | CYP27A1 | 1593 | cytochrome P450 family 27 subfamily A member 1 | Q02318 |
C0004096 | Asthma | CYP27A1 | 1593 | cytochrome P450 family 27 subfamily A member 1 | Q02318 |
C4721453 | Peripheral Nervous System Diseases | CYP27A1 | 1593 | cytochrome P450 family 27 subfamily A member 1 | Q02318 |
C0028754 | Obesity | CYP27A1 | 1593 | cytochrome P450 family 27 subfamily A member 1 | Q02318 |
C0151313 | Sensory neuropathy | CYP27A1 | 1593 | cytochrome P450 family 27 subfamily A member 1 | Q02318 |
C0007222 | Cardiovascular Diseases | CYP27A1 | 1593 | cytochrome P450 family 27 subfamily A member 1 | Q02318 |
C0027066 | Myoclonus | CYP27A1 | 1593 | cytochrome P450 family 27 subfamily A member 1 | Q02318 |
C1956346 | Coronary Artery Disease | CYP27A1 | 1593 | cytochrome P450 family 27 subfamily A member 1 | Q02318 |
C0027765 | nervous system disorder | CYP27A1 | 1593 | cytochrome P450 family 27 subfamily A member 1 | Q02318 |
C0393720 | Reflex Epilepsy, Photosensitive | CYP27A1 | 1593 | cytochrome P450 family 27 subfamily A member 1 | Q02318 |
C1621958 | Glioblastoma Multiforme | CYP27A1 | 1593 | cytochrome P450 family 27 subfamily A member 1 | Q02318 |
C0010068 | Coronary heart disease | CYP27A1 | 1593 | cytochrome P450 family 27 subfamily A member 1 | Q02318 |
C0242379 | Malignant neoplasm of lung | CYP27A1 | 1593 | cytochrome P450 family 27 subfamily A member 1 | Q02318 |
C3714756 | Intellectual Disability | CYP27A1 | 1593 | cytochrome P450 family 27 subfamily A member 1 | Q02318 |
C0017638 | Glioma | BDH1 | 622 | 3-hydroxybutyrate dehydrogenase 1 | Q02338 |
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Last updated: August 19, 2024