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 |
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DisGeNET | July 29, 2024 |
Disease ID | Disease Name | Gene Symbol | Gene ID | Gene Name | UniProt ID ▲ |
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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