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Kidney Tissue Atlas Ontology
Last uploaded:
March 16, 2024
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| Preferred Name | familial restrictive cardiomyopathy | |
| Synonyms |
hereditary restrictive cardiomyopathy |
|
| Definitions |
An instance of restrictive cardiomyopathy that is caused by an inherited modification of the individual's genome. |
|
| ID |
http://purl.obolibrary.org/obo/MONDO_0016340 |
|
| conformsTo |
http://purl.obolibrary.org/obo/mondo/patterns/hereditary.yaml |
|
| database_cross_reference |
Orphanet:217635 SCTID:233878008 ICD9:425.4 OMIMPS:115210
|
|
| exactMatch |
http://linkedlifedata.com/resource/umls/id/C0340429 |
|
| has exact synonym |
hereditary restrictive cardiomyopathy
|
|
| id |
MONDO:0016340
|
|
| imported from | ||
| in_subset |
http://purl.oboInOwllibrary.org/oboInOwl/mondo#ordo_group_of_disorders |
|
| label |
familial restrictive cardiomyopathy
|
|
| notation |
MONDO:0016340
|
|
| prefLabel |
familial restrictive cardiomyopathy
|
|
| should_conform_to |
http://purl.obolibrary.org/obo/mondo/patterns/OMIM_phenotypic_series.yaml |
|
| textual definition |
An instance of restrictive cardiomyopathy that is caused by an inherited modification of the individual's genome.
|
|
| subClassOf |
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