Preferred Name | hypertrophic cardiomyopathy | |
Synonyms |
|
|
Definitions |
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. Xref MGI. OMIM mapping confirmed by DO. [SN]. |
|
ID |
http://purl.obolibrary.org/obo/DOID_11984 |
|
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 |
|
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 |
|
hasExactSynonym |
hypertrophic obstructive cardiomyopathy familial hypertrophic cardiomyopathy |
|
hasOBONamespace |
disease_ontology |
|
id |
DOID:11984 |
|
imported from | ||
label |
hypertrophic cardiomyopathy |
|
prefixIRI |
DOID:11984 |
|
prefLabel |
hypertrophic cardiomyopathy |
|
subClassOf |