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 |
---|---|---|---|---|---|
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 |
C0238033 | Carcinoma of Male Breast | CYP19A1 | 1588 | cytochrome P450 family 19 subfamily A member 1 | P11511 |
C0549622 | Sexual Dysfunction | CYP19A1 | 1588 | cytochrome P450 family 19 subfamily A member 1 | P11511 |
C0238461 | Anaplastic thyroid carcinoma | CYP19A1 | 1588 | cytochrome P450 family 19 subfamily A member 1 | P11511 |
C1153706 | Endometrial adenocarcinoma | CYP19A1 | 1588 | cytochrome P450 family 19 subfamily A member 1 | P11511 |
C0345967 | Malignant mesothelioma | CYP19A1 | 1588 | cytochrome P450 family 19 subfamily A member 1 | P11511 |
C0021364 | Male infertility | CYP19A1 | 1588 | cytochrome P450 family 19 subfamily A member 1 | P11511 |
C0085083 | Ovarian Hyperstimulation Syndrome | CYP19A1 | 1588 | cytochrome P450 family 19 subfamily A member 1 | P11511 |
C0002736 | Amyotrophic Lateral Sclerosis | CYP19A1 | 1588 | cytochrome P450 family 19 subfamily A member 1 | P11511 |
C1336708 | Testicular Germ Cell Tumor | CYP19A1 | 1588 | cytochrome P450 family 19 subfamily A member 1 | P11511 |
C0206081 | Hyperandrogenism | CYP19A1 | 1588 | cytochrome P450 family 19 subfamily A member 1 | P11511 |
C0042133 | Uterine Fibroids | CYP19A1 | 1588 | cytochrome P450 family 19 subfamily A member 1 | P11511 |
C0086132 | Depressive Symptoms | CYP19A1 | 1588 | cytochrome P450 family 19 subfamily A member 1 | P11511 |
C0007286 | Carpal Tunnel Syndrome | CYP19A1 | 1588 | cytochrome P450 family 19 subfamily A member 1 | P11511 |
C0000889 | Acanthosis Nigricans | CYP19A1 | 1588 | cytochrome P450 family 19 subfamily A member 1 | P11511 |
C0549473 | Thyroid carcinoma | CYP19A1 | 1588 | cytochrome P450 family 19 subfamily A member 1 | P11511 |
C1269683 | Major Depressive Disorder | CYP19A1 | 1588 | cytochrome P450 family 19 subfamily A member 1 | P11511 |
C0001418 | Adenocarcinoma | CYP19A1 | 1588 | cytochrome P450 family 19 subfamily A member 1 | P11511 |
C0033375 | Prolactinoma | CYP19A1 | 1588 | cytochrome P450 family 19 subfamily A member 1 | P11511 |
C0271650 | Impaired glucose tolerance | CYP19A1 | 1588 | cytochrome P450 family 19 subfamily A member 1 | P11511 |
C0029463 | Osteosarcoma | CYP19A1 | 1588 | cytochrome P450 family 19 subfamily A member 1 | P11511 |
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Last updated: August 19, 2024