Endocardial fibroelastosis
Symptom Information:
Symptom ID: | HPO:0001706 | ||||||||
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) Abnormality of the endocardium(HPO:0004306) Endocardial fibroelastosis(HPO:0001706) MedDRA: Cardiac disorders(MedDRA:10007541) Endocardial disorders(MedDRA:10014662) Endocardial disorders NEC(MedDRA:10014660) Endocardial fibroelastosis(HPO:0001706) |
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Database Frequency: | 20 / 7739 | ||||||||
Resource: |
All diseases associated with this symptom:
Alström syndrome | (Orphanet:64) |
Atrial standstill | (Orphanet:1344) |
Atrial standstill 1 | (OMIM:108770) |
Barth syndrome | (Orphanet:111) |
Cardiomyopathy, dilated, 1AA with or without left ventricular noncompaction | (OMIM:612158) |
Cardiomyopathy, dilated, 1D | (OMIM:601494) |
Cardiomyopathy, dilated, 1FF | (OMIM:613286) |
Cardiomyopathy, dilated, 1M | (OMIM:607482) |
Cardiomyopathy, familial restrictive, 1 | (OMIM:115210) |
Carnitine uptake deficiency | (Orphanet:158) |
Congenital heart block | (Orphanet:60041) |
ENDOCARDIAL FIBROELASTOSIS AND COARCTATION OF ABDOMINAL AORTA | (OMIM:226100) |
Endomyocardial fibroelastosis | (Orphanet:2022) |
Faciocardiorenal syndrome | (Orphanet:1973) |
HEC syndrome | (Orphanet:2119) |
Histiocytoid cardiomyopathy | (Orphanet:137675) |
Hurler syndrome | (Orphanet:93473) |
Hypoplastic left heart syndrome 1 | (OMIM:241550) |
Mucopolysaccharidosis type 1 | (Orphanet:579) |
ULNAR AGENESIS AND ENDOCARDIAL FIBROELASTOSIS | (OMIM:276822) |