Search Ontology:
Human Disease

infantile hypertrophic cardiomyopathy

Term ID
DOID:0111753
Synonyms
Definition
A hypertrophic cardiomyopathy characterized by isolated hypertrophic cardiomyopathy and congestive heart failure that has_material_basis_in mutation in the overlapping mitochondrial genes MTATP6 and MTATP8. https://www.ncbi.nlm.nih.gov/pubmed/19188198
References
Ontology
Human Disease   ( DOID:0111753 )
Relationships
is a type of
Other Pages
Alliance (1)
Genes Involved
Zebrafish Models
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