hypertrophic cardiomyopathy 3
Information
- Disease name
- hypertrophic cardiomyopathy 3
- Disease ID
- DOID:0110309
- Description
- "A familial hypertrophic cardiomyopathy that has_material_basis_in heterozygous mutation in the alpha-tropomyosin gene (TPM1) on chromosome 15q22." [url:https\://www.ncbi.nlm.nih.gov/pubmed/8205619]
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:115196
- Exact Synonym (Disease Ontology)
- cardiomyopathy familial hypertrophic 3
- Exact Synonym (Disease Ontology)
- CMH3