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 13126 - 13150 of 62743 in total
Disease ID Disease Name Gene Symbol Gene ID Gene Name UniProt ID ▼
C0162871 Aortic Aneurysm, Abdominal ARSI 340075 arylsulfatase family member I Q5FYB1
C0015397 Disorder of eye ARSI 340075 arylsulfatase family member I Q5FYB1
C0678222 Breast Carcinoma ARSI 340075 arylsulfatase family member I Q5FYB1
C0038436 Post-Traumatic Stress Disorder ARSI 340075 arylsulfatase family member I Q5FYB1
C0027651 Neoplasms ARSI 340075 arylsulfatase family member I Q5FYB1
C0086132 Depressive Symptoms ARSI 340075 arylsulfatase family member I Q5FYB1
C0000768 Congenital Abnormality ARSH 347527 arylsulfatase family member H Q5FYA8
C0019158 Hepatitis ARSH 347527 arylsulfatase family member H Q5FYA8
C0023434 Chronic Lymphocytic Leukemia ARSH 347527 arylsulfatase family member H Q5FYA8
C0268263 Multiple Sulfatase Deficiency Disease ARSH 347527 arylsulfatase family member H Q5FYA8
C0026703 Mucopolysaccharidoses ARSH 347527 arylsulfatase family member H Q5FYA8
C0006826 Malignant Neoplasms ARSH 347527 arylsulfatase family member H Q5FYA8
C0406775 Symmetrical dyschromatosis of extremities ARSH 347527 arylsulfatase family member H Q5FYA8
C0023890 Liver Cirrhosis ARSH 347527 arylsulfatase family member H Q5FYA8
C3463824 MYELODYSPLASTIC SYNDROME ARSH 347527 arylsulfatase family member H Q5FYA8
C0700095 Central neuroblastoma ARSH 347527 arylsulfatase family member H Q5FYA8
C0023891 Liver Cirrhosis, Alcoholic ARSH 347527 arylsulfatase family member H Q5FYA8
C0027819 Neuroblastoma ARSH 347527 arylsulfatase family member H Q5FYA8
C0026705 Mucopolysaccharidosis II ARSH 347527 arylsulfatase family member H Q5FYA8
C1332977 Childhood Leukemia ARSH 347527 arylsulfatase family member H Q5FYA8
C3875321 Inflammatory dermatosis ARSH 347527 arylsulfatase family member H Q5FYA8
C0023418 leukemia ARSH 347527 arylsulfatase family member H Q5FYA8
C0023895 Liver diseases ARSH 347527 arylsulfatase family member H Q5FYA8
C0018818 Ventricular Septal Defects ARSH 347527 arylsulfatase family member H Q5FYA8
C0028860 Oculocerebrorenal Syndrome ARSH 347527 arylsulfatase family member H Q5FYA8

About Release Notes Help Feedback

Click here to visit the beta site.


International Collaboration

GlyCosmos is a member of the GlySpace Alliance together with GlyGen and Glycomics@ExPASy.

Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

Partly supported by NIH Common Fund Grant #1U01GM125267-01


Logo License Policies Site Map

Contact: support@glycosmos.org

This work is licensed under Creative Commons Attribution 4.0 International


GlyCosmos Portal v4.0.0

Last updated: August 19, 2024