dilated cardiomyopathy 1S

Summary
Synonym
  • CMD1S
Definition
A dilated cardiomyopathy that has_material_basis_in mutation in the MYH7 gene on chromosome 14q12.
Super Class
autosomal dominant disease dilated cardiomyopathy
External Links
Disease Ontology
DOID:0110454
Mondo Disease Ontology
OMIM
Related Genes
Displaying entries 1 - 10 of 41 in total
Gene ID Gene Symbol Description Source
37 ACADVL acyl-CoA dehydrogenase very long chain
622 BDH1 3-hydroxybutyrate dehydrogenase 1
1120 CHKB choline kinase beta
1376 CPT2 carnitine palmitoyltransferase 2
1605 DAG1 dystroglycan 1
1636 ACE angiotensin I converting enzyme
2194 FASN fatty acid synthase
2218 FKTN fukutin
2720 GLB1 galactosidase beta 1
2876 GPX1 glutathione peroxidase 1
The Human Phenotype Ontology
Displaying entries 1 - 10 of 12 in total
HPO ID HPO Term
HP:0000407 Sensorineural hearing impairment
HP:0000969 Edema
HP:0001635 Congestive heart failure
HP:0001644 Dilated cardiomyopathy
HP:0001727 Thromboembolic stroke
HP:0002875 Exertional dyspnea
HP:0003198 Myopathy
HP:0003457 EMG abnormality
HP:0011675 Arrhythmia
HP:0012378 Fatigue
Displaying all 3 entries
Gene ID Gene Symbol Description
22845 DOLK dolichol kinase
6389 SDHA succinate dehydrogenase complex flavoprotein subunit A
2218 FKTN fukutin

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