Cardiomyopathy, dilated, 1H

General Information (adopted from Orphanet):

Synonyms, Signs: CDM1H
Number of Symptoms 1
OrphanetNr:
OMIM Id: 604288
ICD-10:
UMLs:
MeSH:
MedDRA:
Snomed:

Prevalence, inheritance and age of onset:

Prevalence: No data available.
Inheritance: Autosomal dominant
10486326 [IBIS]
Age of onset:

Disease classification (adopted from Orphanet):

Parent Diseases: Familial isolated dilated cardiomyopathy
 -Rare cardiac disease
 -Rare genetic disease

Symptom Information: Sort by abundance 

1
 (HPO:0001644) Dilated cardiomyopathy 10486326 IBIS 141 / 7739

Associated genes:

locus 2q14-q2;

ClinVar (via SNiPA)

Gene symbol Variation Clinical significance Reference

Additional Information: