Cardiomyopathy, dilated, 1K

General Information (adopted from Orphanet):

Synonyms, Signs: CMD1K
Number of Symptoms 1
OrphanetNr:
OMIM Id: 605582
ICD-10:
UMLs:
MeSH:
MedDRA:
Snomed:

Prevalence, inheritance and age of onset:

Prevalence: No data available.
Inheritance: Autosomal dominant
11085912 [IBIS]
Age of onset:

Disease classification (adopted from Orphanet):

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

Comment:

Cardiomyopathy, dilated, 1K is caused by mutation in locus 6q12-q16 (PMID:11085912).

Symptom Information: Sort by abundance 

1
 (HPO:0001644) Dilated cardiomyopathy 11085912 IBIS 141 / 7739

Associated genes:

locus 6q12-q16;

ClinVar (via SNiPA)

Gene symbol Variation Clinical significance Reference

Additional Information: