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 ▼ |
---|---|---|---|---|---|
C0026848 | Myopathy | CYP3A4 | 1576 | cytochrome P450 family 3 subfamily A member 4 | P08684 |
C0023467 | Leukemia, Myelocytic, Acute | CYP3A4 | 1576 | cytochrome P450 family 3 subfamily A member 4 | P08684 |
C0029456 | Osteoporosis | CYP3A4 | 1576 | cytochrome P450 family 3 subfamily A member 4 | P08684 |
C0271561 | Somatotropin deficiency | CYP3A4 | 1576 | cytochrome P450 family 3 subfamily A member 4 | P08684 |
C0024299 | Lymphoma | CYP3A4 | 1576 | cytochrome P450 family 3 subfamily A member 4 | P08684 |
C0026764 | Multiple Myeloma | CYP3A4 | 1576 | cytochrome P450 family 3 subfamily A member 4 | P08684 |
C0034494 | Rabies (disorder) | CYP3A4 | 1576 | cytochrome P450 family 3 subfamily A member 4 | P08684 |
C0238052 | Xanthomatosis, Cerebrotendinous | CYP3A4 | 1576 | cytochrome P450 family 3 subfamily A member 4 | P08684 |
C0549473 | Thyroid carcinoma | CYP3A4 | 1576 | cytochrome P450 family 3 subfamily A member 4 | P08684 |
C0023895 | Liver diseases | CYP3A4 | 1576 | cytochrome P450 family 3 subfamily A member 4 | P08684 |
C0496870 | Benign neoplasm of liver | CYP3A4 | 1576 | cytochrome P450 family 3 subfamily A member 4 | P08684 |
C1458155 | Mammary Neoplasms | CYP3A4 | 1576 | cytochrome P450 family 3 subfamily A member 4 | P08684 |
C0027051 | Myocardial Infarction | CYP3A4 | 1576 | cytochrome P450 family 3 subfamily A member 4 | P08684 |
C0005684 | Malignant neoplasm of urinary bladder | CYP3A4 | 1576 | cytochrome P450 family 3 subfamily A member 4 | P08684 |
C0035579 | Rickets | CYP3A4 | 1576 | cytochrome P450 family 3 subfamily A member 4 | P08684 |
C0003873 | Rheumatoid Arthritis | CYP3A4 | 1576 | cytochrome P450 family 3 subfamily A member 4 | P08684 |
C0011849 | Diabetes Mellitus | CYP3A4 | 1576 | cytochrome P450 family 3 subfamily A member 4 | P08684 |
C0035078 | Kidney Failure | CYP3A4 | 1576 | cytochrome P450 family 3 subfamily A member 4 | P08684 |
C0040034 | Thrombocytopenia | CYP3A4 | 1576 | cytochrome P450 family 3 subfamily A member 4 | P08684 |
C4721453 | Peripheral Nervous System Diseases | CYP3A4 | 1576 | cytochrome P450 family 3 subfamily A member 4 | P08684 |
C0023890 | Liver Cirrhosis | CYP3A4 | 1576 | cytochrome P450 family 3 subfamily A member 4 | P08684 |
C0220748 | Cartilage-hair hypoplasia | CYP3A4 | 1576 | cytochrome P450 family 3 subfamily A member 4 | P08684 |
C0040136 | Thyroid Neoplasm | CYP3A4 | 1576 | cytochrome P450 family 3 subfamily A member 4 | P08684 |
C0027726 | Nephrotic Syndrome | CYP3A4 | 1576 | cytochrome P450 family 3 subfamily A member 4 | P08684 |
C0019158 | Hepatitis | CYP3A4 | 1576 | cytochrome P450 family 3 subfamily A member 4 | P08684 |
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