[DEL] Familial restrictive cardiomyopathy type 1

General Information (adopted from Orphanet):

Synonyms, Signs:
Number of Symptoms 0
OrphanetNr: 99985
OMIM Id:
ICD-10:
UMLs:
MeSH:
MedDRA:
Snomed:

Prevalence, inheritance and age of onset:

Prevalence: <= 9 of 100 000
Inheritance: Autosomal dominant
Age of onset:

Disease classification (adopted from Orphanet):

Parent Diseases: No data available.

Symptom Information: Sort by abundance 

Associated genes:

ClinVar (via SNiPA)

Gene symbol Variation Clinical significance Reference

Additional Information: