DisGeNET

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
Displaying entries 9076 - 9100 of 62743 in total
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