| Human Disease |
Term: Cardiomyopathy, Familial Hypertrophic, 2; CMH2
OMIM ID: 115195
|
| Associated Genes |
Orthologous mouse and human markers where mutations in one or both species have been associated with phenotypes characteristic of this disease.
Mouse Gene |
Human Gene |
|
Characteristics of this human disease are associated with mutations in... |
| |
|
|
|
|
 ...the human gene.
MGI data currently do not associate this disease with mutations in the orthologous mouse gene. |
| |
|
|
|
Transgenes and
other mutation types |
|
Mouse Models
|
1Models involving transgenes or other mutation types may also appear in other sections of the table.
|
Analysis Tools