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 14051 - 14075 of 62743 in total
Disease ID Disease Name Gene Symbol Gene ID Gene Name UniProt ID ▲
C4721610 Carcinoma, Ovarian Epithelial ADH4 127 alcohol dehydrogenase 4 (class II), pi polypeptide P08319
C0546837 Malignant neoplasm of esophagus ADH4 127 alcohol dehydrogenase 4 (class II), pi polypeptide P08319
C0677886 Epithelial ovarian cancer ADH4 127 alcohol dehydrogenase 4 (class II), pi polypeptide P08319
C0235974 Pancreatic carcinoma ADH4 127 alcohol dehydrogenase 4 (class II), pi polypeptide P08319
C0400966 Non-alcoholic Fatty Liver Disease ADH4 127 alcohol dehydrogenase 4 (class II), pi polypeptide P08319
C1333620 Flat Ductal Epithelial Atypia of the Breast ADH4 127 alcohol dehydrogenase 4 (class II), pi polypeptide P08319
C1850598 Leigh Syndrome due to Mitochondrial Complex III Deficiency PDHA1 5160 pyruvate dehydrogenase E1 subunit alpha 1 P08559
C0026650 Movement Disorders PDHA1 5160 pyruvate dehydrogenase E1 subunit alpha 1 P08559
C0023264 Leigh Disease PDHA1 5160 pyruvate dehydrogenase E1 subunit alpha 1 P08559
C2931891 Necrotizing encephalopathy, infantile subacute, of Leigh PDHA1 5160 pyruvate dehydrogenase E1 subunit alpha 1 P08559
C0034345 Pyruvate Dehydrogenase Complex Deficiency Disease PDHA1 5160 pyruvate dehydrogenase E1 subunit alpha 1 P08559
C0600139 Prostate carcinoma PDHA1 5160 pyruvate dehydrogenase E1 subunit alpha 1 P08559
C0751651 Mitochondrial Diseases PDHA1 5160 pyruvate dehydrogenase E1 subunit alpha 1 P08559
C1850600 Leigh Syndrome due to Mitochondrial Complex V Deficiency PDHA1 5160 pyruvate dehydrogenase E1 subunit alpha 1 P08559
C0001125 Acidosis, Lactic PDHA1 5160 pyruvate dehydrogenase E1 subunit alpha 1 P08559
C0007758 Cerebellar Ataxia PDHA1 5160 pyruvate dehydrogenase E1 subunit alpha 1 P08559
C0005745 Blepharoptosis PDHA1 5160 pyruvate dehydrogenase E1 subunit alpha 1 P08559
C1850597 Leigh Syndrome Due To Mitochondrial Complex II Deficiency PDHA1 5160 pyruvate dehydrogenase E1 subunit alpha 1 P08559
C0235946 Cerebral atrophy PDHA1 5160 pyruvate dehydrogenase E1 subunit alpha 1 P08559
C1839413 Pyruvate Dehydrogenase E1 Alpha Deficiency PDHA1 5160 pyruvate dehydrogenase E1 subunit alpha 1 P08559
C0038379 Strabismus PDHA1 5160 pyruvate dehydrogenase E1 subunit alpha 1 P08559
C0024623 Malignant neoplasm of stomach PDHA1 5160 pyruvate dehydrogenase E1 subunit alpha 1 P08559
C0020555 Hypertrichosis PDHA1 5160 pyruvate dehydrogenase E1 subunit alpha 1 P08559
C1838951 LEIGH SYNDROME DUE TO MITOCHONDRIAL COMPLEX I DEFICIENCY PDHA1 5160 pyruvate dehydrogenase E1 subunit alpha 1 P08559
C0006826 Malignant Neoplasms PDHA1 5160 pyruvate dehydrogenase E1 subunit alpha 1 P08559

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