hypertrophic cardiomyopathy 1
Information
- Disease name
- hypertrophic cardiomyopathy 1
- Disease ID
- DOID:0110307
- Description
- "A familial hypertrophic cardiomyopathy that has_material_basis_in heterozygous mutation in the MYH7 gene on chromosome 14q12." [url:https\://www.ncbi.nlm.nih.gov/pubmed/1975517]
Disease area statistics
[No Data.]
Chromosome band
[No Data.]
Annotation
Genes | Mutation | Description | Source | Links |
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- Disase is a (Disease Ontology)
- DOID:0080326
- Cross Reference ID (Disease Ontology)
- MIM:192600
- Exact Synonym (Disease Ontology)
- cardiomyopathy, familial hypertrophic 1
- Exact Synonym (Disease Ontology)
- CMH1
- Exact Synonym (Disease Ontology)
- hypertrophic cardiomyopathy 19