loading...| Preferred Name | familial cardiomyopathy | |
| Synonyms |
familial cardiomyopathy Primary familial cardiomyopathy hereditary cardiomyopathy Familial cardiomyopathy (disorder) |
|
| Definitions |
An instance of cardiomyopathy that is caused by an inherited modification of the individual's genome. |
|
| ID |
http://www.ebi.ac.uk/efo/EFO_0002945 |
|
| database_cross_reference |
UMLS:C0264789 icd11.foundation:1018022925 MEDGEN:538845 OMIM:115200 SNOMEDCT:35728003 SCTID:35728003 MONDO:0005217 ICD9:425.4 |
|
| definition |
An instance of cardiomyopathy that is caused by an inherited modification of the individual's genome. |
|
| has_exact_synonym |
familial cardiomyopathy Primary familial cardiomyopathy hereditary cardiomyopathy Familial cardiomyopathy (disorder) |
|
| id |
EFO:0002945 |
|
| in_subset |
http://purl.obolibrary.org/obo/mondo/mondo-base#rare |
|
| label |
familial cardiomyopathy |
|
| notation |
EFO:0002945 |
|
| preferred label |
familial cardiomyopathy |
|
| prefLabel |
familial cardiomyopathy |
|
| skos_exactMatch |
http://purl.obolibrary.org/obo/EFO_0002945 http://linkedlifedata.com/resource/umls/id/C0264789 http://identifiers.org/medgen/538845 http://purl.obolibrary.org/obo/mondo/sources/icd11foundation/1018022925 |
|
| term editor |
Tomasz Adamusiak |
|
| subClassOf |