hypertrophic cardiomyopathy 7
Information
- Disease name
- hypertrophic cardiomyopathy 7
- Disease ID
- DOID:0110313
- Description
- "A familial hypertrophic cardiomyopathy that has_material_basis_in heterozygous mutation in the TNNI3 gene on chromosome 19q13.4." [url:https\://www.ncbi.nlm.nih.gov/pubmed/9241277]
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:613690
- Exact Synonym (Disease Ontology)
- cardiomyopathy, familial hypertrophic 7
- Exact Synonym (Disease Ontology)
- CMH7