Restrictive cardiomyopathy
General Information (adopted from Orphanet):
|
Synonyms, Signs:
|
|
|
Number of Symptoms
|
0
|
|
OrphanetNr:
|
217632
|
|
OMIM Id:
|
|
|
ICD-10:
|
|
|
UMLs:
|
C0007196
|
|
MeSH:
|
D002313
|
|
MedDRA:
|
10038748
|
|
Snomed:
|
415295002
90828009
|
Prevalence, inheritance and age of onset:
|
Prevalence:
|
No data available.
|
|
Inheritance:
|
|
|
Age of onset:
|
|
Disease classification (adopted from Orphanet):
|
Parent Diseases:
|
Cardiomyopathy
-Rare cardiac disease
|
Comment:
| This term does not characterize a disease but a group of diseases. Annotations can be found at a more specific level.
|
|
|
|
|
|
|
|
|
|
ClinVar (via SNiPA)
| Gene symbol |
Variation |
Clinical significance |
Reference |