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 9676 - 9700 of 62743 in total
Disease ID Disease Name Gene Symbol Gene ID Gene Name ▲ UniProt ID
C0026848 Myopathy ACADVL 37 acyl-CoA dehydrogenase very long chain P49748
C3150275 COMPLEMENT COMPONENT 2 DEFICIENCY ACADVL 37 acyl-CoA dehydrogenase very long chain P49748
C0020598 Hypocalcemia ACADVL 37 acyl-CoA dehydrogenase very long chain P49748
C0282160 Aplasia Cutis Congenita ACADVL 37 acyl-CoA dehydrogenase very long chain P49748
C2711227 Steatohepatitis ACADVL 37 acyl-CoA dehydrogenase very long chain P49748
C0206667 Adrenal Cortical Adenoma ACADVL 37 acyl-CoA dehydrogenase very long chain P49748
C0524620 Metabolic Syndrome X ACADVL 37 acyl-CoA dehydrogenase very long chain P49748
C0007193 Cardiomyopathy, Dilated ACADVL 37 acyl-CoA dehydrogenase very long chain P49748
C3150651 FATTY LIVER DISEASE, NONALCOHOLIC, SUSCEPTIBILITY TO, 2 ACADVL 37 acyl-CoA dehydrogenase very long chain P49748
C2750440 FATTY LIVER DISEASE, NONALCOHOLIC, SUSCEPTIBILITY TO, 1 ACADVL 37 acyl-CoA dehydrogenase very long chain P49748
C3875321 Inflammatory dermatosis ACADVL 37 acyl-CoA dehydrogenase very long chain P49748
C0220994 Hyperammonemia ACADVL 37 acyl-CoA dehydrogenase very long chain P49748
C0235991 Small for gestational age (disorder) ACADVL 37 acyl-CoA dehydrogenase very long chain P49748
C0221757 alpha 1-Antitrypsin Deficiency ACADVL 37 acyl-CoA dehydrogenase very long chain P49748
C0032285 Pneumonia ACADVL 37 acyl-CoA dehydrogenase very long chain P49748
C0241005 Creatine phosphokinase serum increased ACADVL 37 acyl-CoA dehydrogenase very long chain P49748
C0020639 Hypoproteinemia ACADVL 37 acyl-CoA dehydrogenase very long chain P49748
C0035410 Rhabdomyolysis ACADVL 37 acyl-CoA dehydrogenase very long chain P49748
C0002395 Alzheimer's Disease ACADVL 37 acyl-CoA dehydrogenase very long chain P49748
C4551472 Hypertrophic obstructive cardiomyopathy ACADVL 37 acyl-CoA dehydrogenase very long chain P49748
C0015695 Fatty Liver ACADVL 37 acyl-CoA dehydrogenase very long chain P49748
C0220981 Metabolic acidosis ACADVL 37 acyl-CoA dehydrogenase very long chain P49748
C0018818 Ventricular Septal Defects ACADVL 37 acyl-CoA dehydrogenase very long chain P49748
C0302280 Adrenogenital Syndrome ACADVL 37 acyl-CoA dehydrogenase very long chain P49748
C0020615 Hypoglycemia ACADVL 37 acyl-CoA dehydrogenase very long chain P49748

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