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 |
---|---|---|---|---|---|
C1527336 | Sjogren's Syndrome | CYP19A1 | 1588 | cytochrome P450 family 19 subfamily A member 1 | P11511 |
C0005684 | Malignant neoplasm of urinary bladder | CYP19A1 | 1588 | cytochrome P450 family 19 subfamily A member 1 | P11511 |
C0086543 | Cataract | CYP19A1 | 1588 | cytochrome P450 family 19 subfamily A member 1 | P11511 |
C1847540 | Azoospermia, Nonobstructive | CYP19A1 | 1588 | cytochrome P450 family 19 subfamily A member 1 | P11511 |
C0699885 | Carcinoma of bladder | CYP19A1 | 1588 | cytochrome P450 family 19 subfamily A member 1 | P11511 |
C0019159 | Hepatitis A | CYP19A1 | 1588 | cytochrome P450 family 19 subfamily A member 1 | P11511 |
C0040136 | Thyroid Neoplasm | CYP19A1 | 1588 | cytochrome P450 family 19 subfamily A member 1 | P11511 |
C0699790 | Colon Carcinoma | CYP19A1 | 1588 | cytochrome P450 family 19 subfamily A member 1 | P11511 |
C0007124 | Noninfiltrating Intraductal Carcinoma | CYP19A1 | 1588 | cytochrome P450 family 19 subfamily A member 1 | P11511 |
C2711227 | Steatohepatitis | CYP19A1 | 1588 | cytochrome P450 family 19 subfamily A member 1 | P11511 |
C0702166 | Acne | CYP19A1 | 1588 | cytochrome P450 family 19 subfamily A member 1 | P11511 |
C0149931 | Migraine Disorders | CYP19A1 | 1588 | cytochrome P450 family 19 subfamily A member 1 | P11511 |
C0015695 | Fatty Liver | CYP19A1 | 1588 | cytochrome P450 family 19 subfamily A member 1 | P11511 |
C1970109 | AROMATASE EXCESS SYNDROME | CYP19A1 | 1588 | cytochrome P450 family 19 subfamily A member 1 | P11511 |
C0086981 | Sicca Syndrome | CYP19A1 | 1588 | cytochrome P450 family 19 subfamily A member 1 | P11511 |
C0011849 | Diabetes Mellitus | CYP19A1 | 1588 | cytochrome P450 family 19 subfamily A member 1 | P11511 |
C0014170 | Endometrial Neoplasms | CYP19A1 | 1588 | cytochrome P450 family 19 subfamily A member 1 | P11511 |
C0410207 | Tubular Aggregate Myopathy | CYP19A1 | 1588 | cytochrome P450 family 19 subfamily A member 1 | P11511 |
C0085580 | Essential Hypertension | CYP19A1 | 1588 | cytochrome P450 family 19 subfamily A member 1 | P11511 |
C1568272 | Tendinopathy | CYP19A1 | 1588 | cytochrome P450 family 19 subfamily A member 1 | P11511 |
C1136382 | Sclerocystic Ovaries | CYP19A1 | 1588 | cytochrome P450 family 19 subfamily A member 1 | P11511 |
C0011860 | Diabetes Mellitus, Non-Insulin-Dependent | CYP19A1 | 1588 | cytochrome P450 family 19 subfamily A member 1 | P11511 |
C0751406 | Post-Traumatic Osteoporosis | CYP19A1 | 1588 | cytochrome P450 family 19 subfamily A member 1 | P11511 |
C0282160 | Aplasia Cutis Congenita | CYP19A1 | 1588 | cytochrome P450 family 19 subfamily A member 1 | P11511 |
C0003850 | Arteriosclerosis | CYP19A1 | 1588 | cytochrome P450 family 19 subfamily A member 1 | P11511 |
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Last updated: August 19, 2024