Preferred Name

Cardiomyopathy, Hypertrophic [Disease/Finding]

Synonyms

Cardiomyopathy, Hypertrophic Obstructive

ID

http://purl.bioontology.org/ontology/NDFRT/N0000000687

altLabel

Cardiomyopathy, Hypertrophic Obstructive

Cardiomyopathy, Hypertrophic

cui

C0007194

Has contraindicated drug

http://purl.bioontology.org/ontology/NDFRT/N0000163624

http://purl.bioontology.org/ontology/NDFRT/N0000190438

http://purl.bioontology.org/ontology/NDFRT/N0000151461

http://purl.bioontology.org/ontology/NDFRT/N0000151458

http://purl.bioontology.org/ontology/NDFRT/N0000147056

http://purl.bioontology.org/ontology/NDFRT/N0000147198

http://purl.bioontology.org/ontology/NDFRT/N0000163626

http://purl.bioontology.org/ontology/NDFRT/N0000023170

http://purl.bioontology.org/ontology/NDFRT/N0000161701

http://purl.bioontology.org/ontology/NDFRT/N0000163625

http://purl.bioontology.org/ontology/NDFRT/N0000146388

http://purl.bioontology.org/ontology/NDFRT/N0000151457

http://purl.bioontology.org/ontology/NDFRT/N0000145817

http://purl.bioontology.org/ontology/NDFRT/N0000161696

http://purl.bioontology.org/ontology/NDFRT/N0000190439

MESH 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).

MESH DUI

D002312

MeSH name

Cardiomyopathy, Hypertrophic

MESH UI

M0003464

NDFRT kind

DISEASE_KIND

notation

N0000000687

NUI

N0000000687

prefLabel

Cardiomyopathy, Hypertrophic [Disease/Finding]

SNOMED CID

233873004

45227007

tui

T047

subClassOf

http://purl.bioontology.org/ontology/NDFRT/N0000000442

Delete Subject Author Type Created
No notes to display