Restrictive cardiomyopathy

Symptom Information:

Symptom ID: HPO:0001723
Synonyms:
Restrictive cardiomyopathy [OMIM:Restrictive cardiomyopathy]
Cardiomyopathy, restrictive [OMIM:Cardiomyopathy, restrictive]
Restrictive cardiomyopathy (in some patients) [OMIM:Restrictive cardiomyopathy (in some patients)]
Restrictive cardiomyopathy (very rare) [OMIM:Restrictive cardiomyopathy (very rare)]
Restrictive cardiomyopathy [MedDRA:10038748]
Quality:
Cross references:
OMIM: "Restrictive cardiomyopathy" [OMIM:Restrictive cardiomyopathy]
OMIM: "Cardiomyopathy, restrictive" [OMIM:Cardiomyopathy, restrictive]
OMIM: "Restrictive cardiomyopathy (in some patients)" [OMIM:Restrictive cardiomyopathy (in some patients)]
OMIM: "Restrictive cardiomyopathy (very rare)" [OMIM:Restrictive cardiomyopathy (very rare)]
Is a (Direct Parents):
HPO         Cardiomyopathy
MedDRA Abnormality of the myocardium
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       Abnormality of the cardiovascular system(HPO:0001626)
          Abnormal heart morphology(HPO:0001627)
             obsolete Malformation of the heart and great vessels(HPO:0002564)
                Abnormality of the myocardium(HPO:0001637)
                   Cardiomyopathy(HPO:0001638)
                      Restrictive cardiomyopathy(HPO:0001723)
MedDRA:
Cardiac disorders(MedDRA:10007541)
    Abnormality of the myocardium(HPO:0001637)
       Restrictive cardiomyopathy(HPO:0001723)
Database Frequency: 22 / 7739
Resource:

All diseases associated with this symptom:

Alström syndrome (Orphanet:64)
CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 26 (OMIM:617047)
Cardiomyopathy, dilated, 1D (OMIM:601494)
Cardiomyopathy, dilated, 1KK (OMIM:615248)
Cardiomyopathy, dilated, 1R (OMIM:613424)
Cardiomyopathy, familial hypertrophic, 2 (OMIM:115195)
Cardiomyopathy, familial hypertrophic, 7 (OMIM:613690)
Cardiomyopathy, familial hypertrophic, 8 (OMIM:608751)
Cardiomyopathy, familial restrictive, 1 (OMIM:115210)
Cardiomyopathy, familial restrictive, 3 (OMIM:612422)
Hemochromatosis, type 2A (OMIM:602390)
Idiopathic hypereosinophilic syndrome (Orphanet:3260)
Intellectual disability-seizures-hypotonia-ophthalmologic-skeletal anomalies syndrome (Orphanet:369837)
Left ventricular noncompaction (Orphanet:54260)
Leprechaunism (Orphanet:508)
Loeffler endocarditis (Orphanet:75566)
Mulibrey nanism (Orphanet:2576)
Muscular dystrophy, Selcen type (Orphanet:199340)
Primary hyperoxaluria type 1 (Orphanet:93598)
Tropical endomyocardial fibrosis (Orphanet:75565)
[DEL] Familial restrictive cardiomyopathy type 1 (Orphanet:99985)
[DEL] PSEUDOXANTHOMA ELASTICUM (OMIM:264800)