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Experimental Factor Ontology
Last uploaded:
December 16, 2024
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| Preferred Name | familial isolated dilated cardiomyopathy | |
| Synonyms |
familial isolated dilated cardiomyopathy familial or idiopathic dilated cardiomyopathy |
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| Definitions |
Familial isolated dilated cardiomyopathy is a rare, genetically heterogeneous cardiac disease characterized by dilatation leading to systolic and diastolic dysfunction of the left and/or right ventricles, causing heart failure or arrhythmia. Term added in response to Mondo restructuring. To be considered for replacement or obsoletion in EFO also. |
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| ID |
http://www.ebi.ac.uk/efo/EFO_0700036 |
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| comment |
Term added in response to Mondo restructuring. To be considered for replacement or obsoletion in EFO also.
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| database_cross_reference |
Orphanet:154 UMLS:CN199609
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|
| definition |
Familial isolated dilated cardiomyopathy is a rare, genetically heterogeneous cardiac disease characterized by dilatation leading to systolic and diastolic dysfunction of the left and/or right ventricles, causing heart failure or arrhythmia.
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| has_exact_synonym |
familial isolated dilated cardiomyopathy familial or idiopathic dilated cardiomyopathy
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| label |
familial isolated dilated cardiomyopathy
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| preferred label |
familial isolated dilated cardiomyopathy
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| prefixIRI |
efo:EFO_0700036
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| prefLabel |
familial isolated dilated cardiomyopathy
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| subClassOf |
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|---|---|---|---|---|
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| Mapping To | Ontology | Source |
|---|---|---|
| http://www.ebi.ac.uk/efo/EFO_0700036 | CCONT | SAME_URI |
| http://www.limics.org/hrdo/rdfns#pat_id_635 | HRDO | LOOM |
| http://www.orpha.net/ORDO/Orphanet_154 | ORDO | LOOM |
| http://purl.obolibrary.org/obo/MONDO_0015470 | DOVES | LOOM |
| http://www.ebi.ac.uk/efo/EFO_0700036 | CCONT | LOOM |