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 14876 - 14900 of 62743 in total
Disease ID Disease Name Gene Symbol Gene ID Gene Name UniProt ID ▲
C1851585 MYELOPROLIFERATIVE DISORDER, CHRONIC, WITH EOSINOPHILIA ANXA5 308 annexin A5 P08758
C0023452 Childhood Acute Lymphoblastic Leukemia ANXA5 308 annexin A5 P08758
C0018799 Heart Diseases ANXA5 308 annexin A5 P08758
C0032580 Adenomatous Polyposis Coli ANXA5 308 annexin A5 P08758
C0151468 Thyroid Gland Follicular Adenoma ANXA5 308 annexin A5 P08758
C0002726 Amyloidosis ANXA5 308 annexin A5 P08758
C0162836 Hidradenitis Suppurativa ANXA5 308 annexin A5 P08758
C0027439 Nasopharyngeal Neoplasms ANXA5 308 annexin A5 P08758
C0334533 Arteriovenous hemangioma ANXA5 308 annexin A5 P08758
C0032460 Polycystic Ovary Syndrome ANXA5 308 annexin A5 P08758
C0699791 Stomach Carcinoma ANXA5 308 annexin A5 P08758
C0034735 Raynaud Phenomenon ANXA5 308 annexin A5 P08758
C0751039 Cockayne Syndrome, Type I ANXA5 308 annexin A5 P08758
C0003873 Rheumatoid Arthritis ANXA5 308 annexin A5 P08758
C0022661 Kidney Failure, Chronic ANXA5 308 annexin A5 P08758
C0010417 Cryptorchidism ANXA5 308 annexin A5 P08758
C0027651 Neoplasms STS 412 steroid sulfatase P08842
C2720163 Placental Steroid Sulfatase Deficiency STS 412 steroid sulfatase P08842
C0162809 Kallmann Syndrome STS 412 steroid sulfatase P08842
C0079588 Ichthyosis, X-Linked STS 412 steroid sulfatase P08842
C0025202 melanoma STS 412 steroid sulfatase P08842
C0476089 Endometrial Carcinoma STS 412 steroid sulfatase P08842
C0036341 Schizophrenia STS 412 steroid sulfatase P08842
C0085574 Palindromic rheumatism STS 412 steroid sulfatase P08842
C1859598 ATAXIA, EARLY-ONSET, WITH OCULOMOTOR APRAXIA AND HYPOALBUMINEMIA STS 412 steroid sulfatase P08842

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Last updated: August 19, 2024