hypertrophic cardiomyopathy 4

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Information
Disease name
hypertrophic cardiomyopathy 4
Disease ID
DOID:0110310
Description
"A familial hypertrophic cardiomyopathy that has_material_basis_in heterozygous, homozygous, or compound heterozygous mutation in the gene encoding cardiac myosin-binding protein C (MYBPC3) on chromosome 11p11." [url:https\://www.ncbi.nlm.nih.gov/pubmed/7493025, url:https\://www.ncbi.nlm.nih.gov/pubmed/7493026]
Disease area statistics
[No Data.]
Chromosome band
[No Data.]
Annotation
Genes Mutation Description Source Links
Disase is a (Disease Ontology)
DOID:0080326
Cross Reference ID (Disease Ontology)
MIM:115197
Exact Synonym (Disease Ontology)
cardiomyopathy, familial hypertrophic, 4
Exact Synonym (Disease Ontology)
CMH4