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 47776 - 47800 of 62743 in total
Disease ID Disease Name Gene Symbol Gene ID Gene Name UniProt ID ▼
C0030409 Paracoccidioidomycosis STS 412 steroid sulfatase P08842
C0007131 Non-Small Cell Lung Carcinoma STS 412 steroid sulfatase P08842
C0023890 Liver Cirrhosis STS 412 steroid sulfatase P08842
C0085669 Acute leukemia STS 412 steroid sulfatase P08842
C0004114 Astrocytoma STS 412 steroid sulfatase P08842
C0282102 Chondrodysplasia punctata, X-linked dominant type STS 412 steroid sulfatase P08842
C0020981 Angioimmunoblastic Lymphadenopathy STS 412 steroid sulfatase P08842
C0020179 Huntington Disease STS 412 steroid sulfatase P08842
C0428791 Aortic valve calcification STS 412 steroid sulfatase P08842
C0023895 Liver diseases STS 412 steroid sulfatase P08842
C0011849 Diabetes Mellitus STS 412 steroid sulfatase P08842
C0026987 Myelofibrosis STS 412 steroid sulfatase P08842
C0024121 Lung Neoplasms STS 412 steroid sulfatase P08842
C0342684 Ocular albinism, type I STS 412 steroid sulfatase P08842
C4551686 Malignant neoplasm of soft tissue STS 412 steroid sulfatase P08842
C0270549 Generalized Anxiety Disorder STS 412 steroid sulfatase P08842
C0014522 Epidermodysplasia Verruciformis STS 412 steroid sulfatase P08842
C0020620 Hypohidrosis STS 412 steroid sulfatase P08842
C3463824 MYELODYSPLASTIC SYNDROME STS 412 steroid sulfatase P08842
C0007134 Renal Cell Carcinoma STS 412 steroid sulfatase P08842
C0870082 Hyperkeratosis STS 412 steroid sulfatase P08842
C0003504 Aortic Valve Insufficiency STS 412 steroid sulfatase P08842
C0266929 Chronic Periodontitis STS 412 steroid sulfatase P08842
C0025517 Metabolic Diseases STS 412 steroid sulfatase P08842
C1704272 Benign Prostatic Hyperplasia STS 412 steroid sulfatase P08842

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Last updated: August 19, 2024