Restrictive cardiomyopathy
Symptom Information:
Symptom ID: | HPO:0001723 | |||||
Synonyms: |
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Cross references: |
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Is a (Direct Parents): |
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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) |
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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) |