Preferred Name |
hypertrophic cardiomyopathy |
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Synonyms |
|
|
Definitions |
Xref MGI. OMIM mapping confirmed by DO. [SN]. An intrinsic cardiomyopathy that has_material_basis_in autosomal dominant inheritance and that is characterized by abnormal thickening (hypertrophy) of the heart without any obvious cause. |
|
ID |
http://purl.obolibrary.org/obo/DOID_11984 |
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comment |
Xref MGI. OMIM mapping confirmed by DO. [SN]. |
|
definition |
An intrinsic cardiomyopathy that has_material_basis_in autosomal dominant inheritance and that is characterized by abnormal thickening (hypertrophy) of the heart without any obvious cause. |
|
hasAlternativeId |
DOID:11986 |
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hasDbXref |
MESH:D002312 ICD9CM:425.1 SNOMEDCT_US_2016_03_01:266301006 NCI:C34449 OMIM:PS192600 SNOMEDCT_US_2016_03_01:389999002 SNOMEDCT_US_2016_03_01:233873004 KEGG:05410 ICD9CM:425.11 SNOMEDCT_US_2016_03_01:389998005 ICD10CM:I42.1 SNOMEDCT_US_2016_03_01:15471000 SNOMEDCT_US_2016_03_01:83978005 MESH:D024741 UMLS_CUI:C0007194 SNOMEDCT_US_2016_03_01:45227007 UMLS_CUI:C0949658 ORDO:155 SNOMEDCT_US_2016_03_01:155351008 NCI:C84773 |
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hasExactSynonym |
hypertrophic obstructive cardiomyopathy familial hypertrophic cardiomyopathy |
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hasOBONamespace |
disease_ontology |
|
id |
DOID:11984 |
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imported from | ||
label |
hypertrophic cardiomyopathy |
|
prefixIRI |
DOID:11984 |
|
prefLabel |
hypertrophic cardiomyopathy |
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subClassOf |
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