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 2476 - 2500 of 62743 in total
Disease ID Disease Name Gene Symbol Gene ID ▲ Gene Name UniProt ID
C0154830 Proliferative diabetic retinopathy HPSE 10855 heparanase Q9Y251
C0279070 Adult Oligodendroglioma HPSE 10855 heparanase Q9Y251
C0023418 leukemia HPSE 10855 heparanase Q9Y251
C0079588 Ichthyosis, X-Linked HPSE 10855 heparanase Q9Y251
C0041696 Unipolar Depression HPSE 10855 heparanase Q9Y251
C0206698 Cholangiocarcinoma HPSE 10855 heparanase Q9Y251
C0007133 Carcinoma, Papillary HPSE 10855 heparanase Q9Y251
C0007130 Mucinous Adenocarcinoma HPSE 10855 heparanase Q9Y251
C0011581 Depressive disorder HPSE 10855 heparanase Q9Y251
C0004779 Basal Cell Nevus Syndrome HPSE 10855 heparanase Q9Y251
C0242584 Autoimmune thrombocytopenia HPSE 10855 heparanase Q9Y251
C0699885 Carcinoma of bladder HPSE 10855 heparanase Q9Y251
C0002395 Alzheimer's Disease CYP46A1 10858 cytochrome P450 family 46 subfamily A member 1 Q9Y6A2
C0494463 Alzheimer Disease, Late Onset CYP46A1 10858 cytochrome P450 family 46 subfamily A member 1 Q9Y6A2
C0949664 Tauopathies CYP46A1 10858 cytochrome P450 family 46 subfamily A member 1 Q9Y6A2
C0006111 Brain Diseases CYP46A1 10858 cytochrome P450 family 46 subfamily A member 1 Q9Y6A2
C0002726 Amyloidosis CYP46A1 10858 cytochrome P450 family 46 subfamily A member 1 Q9Y6A2
C0339573 Glaucoma, Primary Open Angle CYP46A1 10858 cytochrome P450 family 46 subfamily A member 1 Q9Y6A2
C0007820 Cerebrovascular Disorders CYP46A1 10858 cytochrome P450 family 46 subfamily A member 1 Q9Y6A2
C0344315 Depressed mood CYP46A1 10858 cytochrome P450 family 46 subfamily A member 1 Q9Y6A2
C0009402 Colorectal Carcinoma CYP46A1 10858 cytochrome P450 family 46 subfamily A member 1 Q9Y6A2
C0278878 Adult Glioblastoma CYP46A1 10858 cytochrome P450 family 46 subfamily A member 1 Q9Y6A2
C0524851 Neurodegenerative Disorders CYP46A1 10858 cytochrome P450 family 46 subfamily A member 1 Q9Y6A2
C0020179 Huntington Disease CYP46A1 10858 cytochrome P450 family 46 subfamily A member 1 Q9Y6A2
C0011265 Presenile dementia CYP46A1 10858 cytochrome P450 family 46 subfamily A member 1 Q9Y6A2

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Last updated: August 19, 2024