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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 |
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| database_cross_reference |
UMLS:C0264789 OMIM:115200 SNOMEDCT:35728003 SCTID:35728003 ICD9:425.4 MONDO:0005217 |
|
| definition |
An instance of cardiomyopathy that is caused by an inherited modification of the individual's genome. |
|
| exactMatch | ||
| 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 |
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| prefLabel |
familial cardiomyopathy |
|
| term editor |
Tomasz Adamusiak |
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| subClassOf |
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