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 48001 - 48025 of 62743 in total
Disease ID Disease Name Gene Symbol ▼ Gene ID Gene Name UniProt ID
C0020538 Hypertensive disease CTSA 5476 cathepsin A P10619
C0085078 Lysosomal Storage Diseases CTSA 5476 cathepsin A P10619
C0018916 Hemangioma CTSA 5476 cathepsin A P10619
C0206638 Giant Cell Tumor of Bone CTSA 5476 cathepsin A P10619
C0010036 Corneal dystrophy CTSA 5476 cathepsin A P10619
C0026697 Mucolipidoses CTSA 5476 cathepsin A P10619
C1800706 Idiopathic Pulmonary Fibrosis CTSA 5476 cathepsin A P10619
C0003486 Aortic Aneurysm CTSA 5476 cathepsin A P10619
C0004096 Asthma CTSA 5476 cathepsin A P10619
C0152013 Adenocarcinoma of lung (disorder) CTSA 5476 cathepsin A P10619
C0085131 Gangliosidosis GM1 CTSA 5476 cathepsin A P10619
C2718068 beta-Galactosidase Deficiency CTSA 5476 cathepsin A P10619
C3711381 Hereditary Diffuse Leukoencephalopathy with Spheroids CTSA 5476 cathepsin A P10619
C0268226 Type I Mucolipidosis CTSA 5476 cathepsin A P10619
C0035078 Kidney Failure CTSA 5476 cathepsin A P10619
C0032285 Pneumonia CTSA 5476 cathepsin A P10619
C2711227 Steatohepatitis CTSA 5476 cathepsin A P10619
C0002986 Fabry Disease CTSA 5476 cathepsin A P10619
C0010038 Corneal Opacity CTSA 5476 cathepsin A P10619
C0019693 HIV Infections CTSA 5476 cathepsin A P10619
C3714636 Pneumonitis CTSA 5476 cathepsin A P10619
C0019348 Herpes Simplex Infections CTSA 5476 cathepsin A P10619
C0013336 Dwarfism CTSA 5476 cathepsin A P10619
C0006826 Malignant Neoplasms CTSA 5476 cathepsin A P10619
C3714756 Intellectual Disability CTSA 5476 cathepsin A P10619

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Last updated: August 19, 2024