Histiocytoid cardiomyopathy

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.

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Narrow down the case reports

Total: 31 (papers)

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Matched Phenotype Gene Mutation MeSH

Rank (Similarity)	PMID (PMCID)
7 (4.0%)	876688	Histiocytoid cardiomyopathy of infancy: an unexplained myofibre degeneration. Bruton D, Herdson PB, Becroft DM. Pathology. 1977;9(2):115-22. [ Show abstract ] [ Hide abstract ]
		Hydrocephalus


		Autopsy Cardiomyopathies Females Homo sapiens Infant Mitochondria Myocardium Myofibrils

Phenotype(s) retrieved from Orphanet

Total: 0

HPO ID	Term	Frequency

Phenotype(s) retrieved from case reports

Total: 11

HPO ID	Term	# of case reports
HP:0011675	Arrhythmia	4
HP:0000568	Microphthalmia	3
HP:0010566	Hamartoma	3
HP:0001638	Cardiomyopathy	2
HP:0001716	Wolff-Parkinson-White syndrome	2
HP:0009729	Cardiac rhabdomyoma	2
HP:0001645	Sudden cardiac death	1
HP:0001695	Cardiac arrest	1
HP:0003128	Lactic acidosis	1
HP:0009730	Rhabdomyoma	1
HP:0010617	Cardiac fibroma	1

Causative gene(s) retrieved from Orphanet

Total: 1

Gene Symbol	Gene Name	Entrez Gene ID
MT-CYB	mitochondrially encoded cytochrome b	4519