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 39251 - 39275 of 62743 in total
Disease ID Disease Name Gene Symbol Gene ID Gene Name UniProt ID ▲
C0013080 Down Syndrome ARSD 414 arylsulfatase D P51689
C0152227 Excessive tearing ARSD 414 arylsulfatase D P51689
C0175702 Williams Syndrome ARSD 414 arylsulfatase D P51689
C1136249 Mental Retardation, X-Linked ARSD 414 arylsulfatase D P51689
C0023434 Chronic Lymphocytic Leukemia ARSD 414 arylsulfatase D P51689
C0036572 Seizures ARSD 414 arylsulfatase D P51689
C0018799 Heart Diseases ARSD 414 arylsulfatase D P51689
C0014544 Epilepsy ARSD 414 arylsulfatase D P51689
C1263846 Attention deficit hyperactivity disorder ARSD 414 arylsulfatase D P51689
C0014175 Endometriosis ARSD 414 arylsulfatase D P51689
C0007194 Hypertrophic Cardiomyopathy ARSD 414 arylsulfatase D P51689
C0011757 Developmental Coordination Disorder ARSD 414 arylsulfatase D P51689
C0013170 Drug habituation ARSD 414 arylsulfatase D P51689
C0034089 Pulmonary Valve Stenosis ARSD 414 arylsulfatase D P51689
C0476254 Dyslexia ARSD 414 arylsulfatase D P51689
C0036857 Severe intellectual disability ARSD 414 arylsulfatase D P51689
C0004352 Autistic Disorder ARSD 414 arylsulfatase D P51689
C0032460 Polycystic Ovary Syndrome ARSD 414 arylsulfatase D P51689
C0175683 Citrullinemia ARSD 414 arylsulfatase D P51689
C0018801 Heart failure ARSD 414 arylsulfatase D P51689
C0236792 Asperger Syndrome ARSD 414 arylsulfatase D P51689
C0011581 Depressive disorder ARSD 414 arylsulfatase D P51689
C0004364 Autoimmune Diseases ARSD 414 arylsulfatase D P51689
C0268548 Hyperargininemia ARSD 414 arylsulfatase D P51689
C0006142 Malignant neoplasm of breast ARSD 414 arylsulfatase D P51689

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Last updated: August 19, 2024