Hearing Loss Disease Portal


 
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Most Common: Hearing Loss (D034381), Deafness (D003638), Sensorineural HL (D006319), Waardenburg Syndrome, Usher Syndromes
Disease Browser
Parent Node:
expandAortic Stenosis, Subvalvular (D001020)
Parent Node:
expandCardiomyopathies (D009202)
..Starting node
..expandCardiomyopathy, Hypertrophic (D002312)

       Child Nodes:
........expandAcyl-CoA Dehydrogenase Family, Member 9, Deficiency of (C567006)
........expandCardioencephalomyopathy, Fatal Infantile, due to Cytochrome C Oxidase Deficiency (C565784)
........expandCardiomyopathy, Hypertrophic, Familial (D024741) Child15
........expandDeafness, Sensorineural, with Hypertrophic Cardiomyopathy (C565236)
........expandLipoatrophy with diabetes, hepatic steatosis, cardiomyopathy, and leukomelanodermic papules (C535905)



 Sister Nodes: 
..expandAlpha-B Crystallinopathy (C563848)
..expandArrhythmogenic Right Ventricular Dysplasia (D019571) Child13
..expandAtaxia, Deafness, and Cardiomyopathy (C565932)
..expandAtrial Standstill (C563984)
..expandCardiac Lipidosis, Familial (C565884)
..expandCardiomyopathy Associated With Myopathy And Sudden Death (C565881)
..expandCardiomyopathy dilated with Woolly hair and keratoderma (C535581)
..expandCardiomyopathy hypogonadism collagenoma syndrome (C535582)
..expandCardiomyopathy, Alcoholic (D002310)
..expandCardiomyopathy, Dilated (D002311) Child40
..expandCardiomyopathy, fatal fetal, due to myocardial calcification (C543241)
..expandCardiomyopathy, Hypertrophic (D002312) Child20
..expandCardiomyopathy, infantile histiocytoid (C535584)
..expandCardiomyopathy, Restrictive (D002313) Child3
..expandCardioneuromyopathy with Hyaline Masses and Nemaline Rods (C564655)
..expandCataract and cardiomyopathy (C538280)
..expandChagas Cardiomyopathy (D002598)
..expandDiabetic Cardiomyopathies (D058065)
..expandEncephalopathy, Axonal, with Necrotizing Myopathy, Cardiomyopathy, and Cataracts (C565596)
..expandEndocardial Fibroelastosis (D004695) Child9
..expandEndomyocardial Fibrosis (D004719)
..expandGlycogen Storage Disease Type IIb (D052120)
..expandHypertaurinuric Cardiomyopathy (C564157)
..expandKearns-Sayre Syndrome (D007625) Child1
..expandKeshan disease (C536166)
..expandMuscular Dystrophy, Cardiac Type (C563247)
..expandMyocardial Reperfusion Injury (D015428)
..expandMyocarditis (D009205)
..expandMyopathy, Early-Onset, with Fatal Cardiomyopathy (C567129)
..expandMyopathy, Myofibrillar, Desmin-Related (C563319)
..expandNajjar syndrome (C535580)
..expandRoifman syndrome (C535866)
..expandSarcoglycanopathies (D058088) Child3
..expandSystemic carnitine deficiency (C536778)
..expandTrifunctional Protein Deficiency With Myopathy And Neuropathy (C566945)
..expandUruguay Faciocardiomusculoskeletal Syndrome (C564544)
   

Human Disease MESH is developed by UMLS.
Further data from MedGen, OMIM, CTD
Term ID:1758
Name:Cardiomyopathy, Hypertrophic
Definition:A form of CARDIAC MUSCLE disease, characterized by left and/or right ventricular hypertrophy (HYPERTROPHY, LEFT VENTRICULAR; HYPERTROPHY, RIGHT VENTRICULAR), frequent asymmetrical involvement of the HEART SEPTUM, and normal or reduced left ventricular volume. Risk factors include HYPERTENSION; AORTIC STENOSIS; and gene MUTATION; (FAMILIAL HYPERTROPHIC CARDIOMYOPATHY).
Alternative IDs:
ParentIDs:MESH:D001020|MESH:D009202
TreeNumbers:C14.280.238.100 |C14.280.484.150.070.160
Synonyms:Cardiomyopathies, Hypertrophic |Cardiomyopathies, Hypertrophic Obstructive |Cardiomyopathy, Hypertrophic Obstructive |Hypertrophic Cardiomyopathies |Hypertrophic Cardiomyopathy |Hypertrophic Obstructive Cardiomyopathies |Hypertrophic Obstructive Cardiomyopathy
Slim Mappings:Cardiovascular disease
Reference: MedGen: D002312
MeSH: D002312
OMIM:

Genes:
Phenotypes
Disease Causing ClinVar Variants