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 41476 - 41500 of 62743 in total
Disease ID Disease Name Gene Symbol Gene ID Gene Name ▼ UniProt ID
C0014544 Epilepsy CYP19A1 1588 cytochrome P450 family 19 subfamily A member 1 P11511
C0699791 Stomach Carcinoma CYP19A1 1588 cytochrome P450 family 19 subfamily A member 1 P11511
C0017638 Glioma CYP19A1 1588 cytochrome P450 family 19 subfamily A member 1 P11511
C0020619 Hypogonadism CYP19A1 1588 cytochrome P450 family 19 subfamily A member 1 P11511
C1834582 MYELOPROLIFERATIVE SYNDROME, TRANSIENT CYP19A1 1588 cytochrome P450 family 19 subfamily A member 1 P11511
C0007115 Malignant neoplasm of thyroid CYP19A1 1588 cytochrome P450 family 19 subfamily A member 1 P11511
C0267785 Leiomyomatosis peritonealis disseminata CYP19A1 1588 cytochrome P450 family 19 subfamily A member 1 P11511
C0020459 Hyperinsulinism CYP19A1 1588 cytochrome P450 family 19 subfamily A member 1 P11511
C0003128 Anovulation CYP19A1 1588 cytochrome P450 family 19 subfamily A member 1 P11511
C0033581 prostatitis CYP19A1 1588 cytochrome P450 family 19 subfamily A member 1 P11511
C0001973 Alcoholic Intoxication, Chronic CYP19A1 1588 cytochrome P450 family 19 subfamily A member 1 P11511
C0042131 Uterine Diseases CYP19A1 1588 cytochrome P450 family 19 subfamily A member 1 P11511
C0007120 Bronchioloalveolar Adenocarcinoma CYP19A1 1588 cytochrome P450 family 19 subfamily A member 1 P11511
C0033677 Protein-Energy Malnutrition CYP19A1 1588 cytochrome P450 family 19 subfamily A member 1 P11511
C0684249 Carcinoma of lung CYP19A1 1588 cytochrome P450 family 19 subfamily A member 1 P11511
C0001787 Osteoporosis, Age-Related CYP19A1 1588 cytochrome P450 family 19 subfamily A member 1 P11511
C0029408 Degenerative polyarthritis CYP19A1 1588 cytochrome P450 family 19 subfamily A member 1 P11511
C1449563 Cardiomyopathy, Familial Idiopathic CYP19A1 1588 cytochrome P450 family 19 subfamily A member 1 P11511
C3203102 Idiopathic pulmonary arterial hypertension CYP19A1 1588 cytochrome P450 family 19 subfamily A member 1 P11511
C0027819 Neuroblastoma CYP19A1 1588 cytochrome P450 family 19 subfamily A member 1 P11511
C0848558 Hypospadias CYP19A1 1588 cytochrome P450 family 19 subfamily A member 1 P11511
C0036631 Seminoma CYP19A1 1588 cytochrome P450 family 19 subfamily A member 1 P11511
C0852036 Pregnancy associated hypertension CYP19A1 1588 cytochrome P450 family 19 subfamily A member 1 P11511
C0011581 Depressive disorder CYP19A1 1588 cytochrome P450 family 19 subfamily A member 1 P11511
C0497327 Dementia CYP19A1 1588 cytochrome P450 family 19 subfamily A member 1 P11511

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Last updated: August 19, 2024