Abnormality of the endocardium

Symptom Information:

Symptom ID: HPO:0004306
Synonyms:
Abnormality of the endomycoardium [HPO:0004306]
Endocardium anomaly [Orphanet:34600]
Endocardium anomalies/fibroelastosis/endocarditis [Orphanet:34600]
Quality:
Cross references:
Orphanet:34600 "Endocardium anomalies/fibroelastosis/endocarditis" [Orphanet:34600]
Is a (Direct Parents):
HPO         Abnormal heart morphology
Orphanet Endocardial fibroelastosis
Orphanet Structural anomalies of the cardio-circulatory system
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)
MedDRA:
Database Frequency: 24 / 7739
Resource:

All diseases associated with this symptom:

Barth syndrome (Orphanet:111)
Behçet disease (Orphanet:117)
Cardiomyopathy, dilated, 1FF (OMIM:613286)
Cardiomyopathy, dilated, 1JJ (OMIM:615235)
Chronic mucocutaneous candidiasis (Orphanet:1334)
Ebstein malformation (Orphanet:1880)
Endomyocardial fibroelastosis (Orphanet:2022)
Eosinophilic granulomatosis with polyangiitis (Orphanet:183)
Fabry disease (Orphanet:324)
Faciocardiorenal syndrome (Orphanet:1973)
HEC syndrome (Orphanet:2119)
Hurler syndrome (Orphanet:93473)
Legionellosis (Orphanet:549)
Marfan syndrome (Orphanet:558)
Mosaic trisomy 9 (Orphanet:99776)
Noonan syndrome with multiple lentigines (Orphanet:500)
Osteogenesis imperfecta (Orphanet:666)
Pseudoxanthoma elasticum (Orphanet:758)
Relapsing polychondritis (Orphanet:728)
Rheumatic fever (Orphanet:3099)
Takayasu arteritis (Orphanet:3287)
Toriello-Carey syndrome (Orphanet:3338)
Uhl anomaly (Orphanet:3403)
Williams syndrome (Orphanet:904)