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 8751 - 8775 of 62743 in total
Disease ID Disease Name Gene Symbol Gene ID ▲ Gene Name UniProt ID
C0034013 Precocious Puberty CYP11B1 1584 cytochrome P450 family 11 subfamily B member 1 P15538
C0015934 Fetal Growth Retardation CYP11B1 1584 cytochrome P450 family 11 subfamily B member 1 P15538
C0085580 Essential Hypertension CYP11B1 1584 cytochrome P450 family 11 subfamily B member 1 P15538
C0678222 Breast Carcinoma CYP11B1 1584 cytochrome P450 family 11 subfamily B member 1 P15538
C0038454 Cerebrovascular accident CYP11B1 1584 cytochrome P450 family 11 subfamily B member 1 P15538
C0029456 Osteoporosis CYP11B1 1584 cytochrome P450 family 11 subfamily B member 1 P15538
C0018799 Heart Diseases CYP11B1 1584 cytochrome P450 family 11 subfamily B member 1 P15538
C0020621 Hypokalemia CYP11B1 1584 cytochrome P450 family 11 subfamily B member 1 P15538
C0032460 Polycystic Ovary Syndrome CYP11B1 1584 cytochrome P450 family 11 subfamily B member 1 P15538
C0206667 Adrenal Cortical Adenoma CYP11B1 1584 cytochrome P450 family 11 subfamily B member 1 P15538
C0013336 Dwarfism CYP11B1 1584 cytochrome P450 family 11 subfamily B member 1 P15538
C0342482 X-linked Adrenal Hypoplasia CYP11B1 1584 cytochrome P450 family 11 subfamily B member 1 P15538
C0027651 Neoplasms CYP11B2 1585 cytochrome P450 family 11 subfamily B member 2 P19099
C0020538 Hypertensive disease CYP11B2 1585 cytochrome P450 family 11 subfamily B member 2 P19099
C0001430 Adenoma CYP11B2 1585 cytochrome P450 family 11 subfamily B member 2 P19099
C0085580 Essential Hypertension CYP11B2 1585 cytochrome P450 family 11 subfamily B member 2 P19099
C3713420 Familial Hyperaldosteronism CYP11B2 1585 cytochrome P450 family 11 subfamily B member 2 P19099
C1384514 Conn Syndrome CYP11B2 1585 cytochrome P450 family 11 subfamily B member 2 P19099
C1260386 Glucocorticoid-remediable aldosteronism CYP11B2 1585 cytochrome P450 family 11 subfamily B member 2 P19099
C0017661 IGA Glomerulonephritis CYP11B2 1585 cytochrome P450 family 11 subfamily B member 2 P19099
C1449563 Cardiomyopathy, Familial Idiopathic CYP11B2 1585 cytochrome P450 family 11 subfamily B member 2 P19099
C0020621 Hypokalemia CYP11B2 1585 cytochrome P450 family 11 subfamily B member 2 P19099
C0740457 Malignant neoplasm of kidney CYP11B2 1585 cytochrome P450 family 11 subfamily B member 2 P19099
C0206686 Adrenocortical carcinoma CYP11B2 1585 cytochrome P450 family 11 subfamily B member 2 P19099
C0018802 Congestive heart failure CYP11B2 1585 cytochrome P450 family 11 subfamily B member 2 P19099

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Last updated: August 19, 2024