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 14976 - 15000 of 62743 in total
Disease ID Disease Name Gene Symbol Gene ID Gene Name ▲ UniProt ID
C0000768 Congenital Abnormality ARSD 414 arylsulfatase D P51689
C0038436 Post-Traumatic Stress Disorder ARSD 414 arylsulfatase D P51689
C4721769 Citrullinemia Type 1 ARSD 414 arylsulfatase D P51689
C0028754 Obesity ARSD 414 arylsulfatase D P51689
C0006142 Malignant neoplasm of breast ARSD 414 arylsulfatase D P51689
C0344724 Ostium secundum atrial septal defect ARSD 414 arylsulfatase D P51689
C0036572 Seizures ARSD 414 arylsulfatase D P51689
C0017601 Glaucoma ARSD 414 arylsulfatase D P51689
C0018802 Congestive heart failure ARSD 414 arylsulfatase D P51689
C0678222 Breast Carcinoma ARSD 414 arylsulfatase D P51689
C0020538 Hypertensive disease ARSD 414 arylsulfatase D P51689
C0268547 Argininosuccinic Aciduria ARSD 414 arylsulfatase D P51689
C0037789 Specific reading disorder ARSD 414 arylsulfatase D P51689
C0009460 Communication impairment ARSD 414 arylsulfatase D P51689
C0476254 Dyslexia ARSD 414 arylsulfatase D P51689
C0003076 Aniridia ARSD 414 arylsulfatase D P51689
C0004364 Autoimmune Diseases ARSD 414 arylsulfatase D P51689
C0007222 Cardiovascular Diseases ARSD 414 arylsulfatase D P51689
C0878544 Cardiomyopathies ARSD 414 arylsulfatase D P51689
C0175695 Sotos' syndrome ARSD 414 arylsulfatase D P51689
C0023186 Learning Disorders ARSD 414 arylsulfatase D P51689
C0004930 Behavior Disorders ARSD 414 arylsulfatase D P51689
C0011757 Developmental Coordination Disorder ARSD 414 arylsulfatase D P51689
C0036857 Severe intellectual disability ARSD 414 arylsulfatase D P51689
C0022672 Acute Kidney Tubular Necrosis ARSD 414 arylsulfatase D P51689

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Last updated: August 19, 2024