Preferred Name | Cardiomyopathy, Hypertrophic [Disease/Finding] | |
Synonyms |
Cardiomyopathy, Hypertrophic Cardiomyopathy, Hypertrophic Obstructive |
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ID |
http://purl.bioontology.org/ontology/NDFRT/N0000000687 |
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altLabel |
Cardiomyopathy, Hypertrophic Cardiomyopathy, Hypertrophic Obstructive |
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cui |
C0007194 |
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Has contraindicated drug |
http://purl.bioontology.org/ontology/NDFRT/N0000163625 http://purl.bioontology.org/ontology/NDFRT/N0000151458 http://purl.bioontology.org/ontology/NDFRT/N0000147056 http://purl.bioontology.org/ontology/NDFRT/N0000146388 http://purl.bioontology.org/ontology/NDFRT/N0000163624 http://purl.bioontology.org/ontology/NDFRT/N0000163626 http://purl.bioontology.org/ontology/NDFRT/N0000145817 http://purl.bioontology.org/ontology/NDFRT/N0000190438 http://purl.bioontology.org/ontology/NDFRT/N0000161696 http://purl.bioontology.org/ontology/NDFRT/N0000151457 http://purl.bioontology.org/ontology/NDFRT/N0000151461 http://purl.bioontology.org/ontology/NDFRT/N0000161701 http://purl.bioontology.org/ontology/NDFRT/N0000147198 |
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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). |
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MESH DUI |
D002312 |
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MeSH name |
Cardiomyopathy, Hypertrophic |
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MESH UI |
M0003464 |
|
NDFRT kind |
DISEASE_KIND |
|
notation |
N0000000687 |
|
NUI |
N0000000687 |
|
prefLabel |
Cardiomyopathy, Hypertrophic [Disease/Finding] |
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SNOMED CID |
45227007 233873004 |
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tui |
T047 |
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subClassOf |