Hearing Loss Disease Portal


 
Switch to table view
Most Common: Hearing Loss (D034381), Deafness (D003638), Sensorineural HL (D006319), Waardenburg Syndrome, Usher Syndromes
Disease Browser
Parent Node:
expand
Barth Syndrome (D056889)
..Starting node
..expand
Noncompaction of Left Ventricular Myocardium, Familial Isolated, X-Linked (C564571)

       Child Nodes:



 Sister Nodes: 
..expandDilated cardiomyopathy, neutropenia, skeletal myopathy, and abnormal mitochondria (C538496)
..expandNoncompaction of Left Ventricular Myocardium, Familial Isolated, X-Linked (C564571)
   

Human Disease MESH is developed by UMLS.
Further data from MedGen, OMIM, CTD
Term ID:8097
Name:Noncompaction of Left Ventricular Myocardium, Familial Isolated, X-Linked
Definition:
Alternative IDs:
ParentIDs:MESH:D056889
TreeNumbers:C14.240.400.172/C564571 |C14.280.400.172/C564571 |C16.131.077.121/C564571 |C16.131.240.400.172/C564571 |C16.320.322.068/C564571 |C16.320.565.398.224/C564571 |C18.452.648.398.224/C564571
Synonyms:Left Ventricular Noncompaction, Isolated, X-Linked
Slim Mappings:Cardiovascular disease|Congenital abnormality|Genetic disease (inborn)|Metabolic disease
Reference: MedGen: C564571
MeSH: C564571
OMIM:

Genes:
Phenotypes
Disease Causing ClinVar Variants