hypertrophic cardiomyopathy 13
Information
- Disease name
- hypertrophic cardiomyopathy 13
- Disease ID
- DOID:0110319
- Description
- "A familial hypertrophic cardiomyopathy that has_material_basis_in heterozygous mutation in the TNNC1 gene on chromosome 3p21." [url:https\://www.ncbi.nlm.nih.gov/pubmed/11385718]
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:613243
- Exact Synonym (Disease Ontology)
- cardiomyopathy familial hypertrophic 13
- Exact Synonym (Disease Ontology)
- CMH13