Term info
- UMLS:CN239812 (MONDO:equivalentTo)
- NCIT:C45745 (MONDO:equivalentTo)
- MESH:C535584 (Orphanet:137675/e)
- GARD:0009511 (MONDO:equivalentTo)
- UMLS:C1708371 (Orphanet:137675/e)
- OMIM:500000 (Orphanet:137675/e)
- Orphanet:137675 (OMIM:500000)
- DOID:0080198 (MONDO:equivalentTo)
gard_rare, ordo_disease
Histiocytoid cardiomyopathy is an arrhythmogenic disorder characterised by cardiomegaly, severe cardiac arrhythmias or sudden death, and the presence of histiocyte-like cells within the myocardium.
http://purl.obolibrary.org/obo/DOID_0080198, http://linkedlifedata.com/resource/umls/id/C1708371, http://purl.obolibrary.org/obo/NCIT_C45745, http://purl.obolibrary.org/obo/Orphanet_137675, https://omim.org/entry/500000, http://linkedlifedata.com/resource/umls/id/CN239812, http://identifiers.org/mesh/C535584
isolated Cardiac lipidosis, infantile cardiomyopathy with histiocytoid change, histiocytoid cardiomyopathy, Purkinje cell hamartoma, congenital cardiomyopathy, oncocytic cardiomyopathy, infantile xanthomatous cardiomyopathy, myocardial hamartoma, Arachnocytosis of the myocardium, foamy myocardial transformation of infancy
cardiomyopathy, focal Lipid, focal lipid cardiomyopathy, cardiomyopathy, oncocytic, cardiomyopathy, infantile histiocytoid, infantile histiocytoid cardiomyopathy, cardiomyopathy, infantile xanthomatous
MONDO:0010771
https://rarediseases.info.nih.gov/diseases/9511/infantile-histiocytoid-cardiomyopathy