Disease #03094 (CMD1AA;CMH23 (cardiomyopathy, dilated, type 1AA (CMD-1AA, cardiomyopathy, hypertrophic, type 23 (CMH-23))), OMIM:612158)
Official abbreviation |
CMD1AA;CMH23 |
Name |
cardiomyopathy, dilated, type 1AA (CMD-1AA, cardiomyopathy, hypertrophic, type 23 (CMH-23)) |
OMIM ID |
612158 |
Human Phenotype Ontology Project (HPO) |
HPO |
Inheritance |
Autosomal dominant |
Individuals reported having this disease |
48 |
Phenotype entries for this disease |
46 |
Associated with 1 gene |
ACTN2 |
Associated tissues |
- |
Disease features |
- |
Remarks |
- |
Date created |
2014-09-25 23:29:40 +02:00 (CEST) |
Date last edited |
2020-05-03 14:15:18 +02:00 (CEST) |
Individuals
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