Left ventricular failure

Symptom Information:

Symptom ID: HPO:0005162
Synonyms:
Left ventricular impairment [HPO:0005162]
Left ventricular impairment [OMIM:Left ventricular impairment]
Quality:
Cross references:
OMIM: "Left ventricular impairment" [OMIM:Left ventricular impairment]
Is a (Direct Parents):
HPO         Abnormality of the left ventricle
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 cardiac ventricle(HPO:0001713)
                   Abnormality of the left ventricle(HPO:0001711)
                      Left ventricular failure(HPO:0005162)
MedDRA:
Database Frequency: 18 / 7739
Resource:

All diseases associated with this symptom:

Autosomal recessive limb-girdle muscular dystrophy type 2C (Orphanet:353)
Autosomal recessive limb-girdle muscular dystrophy type 2D (Orphanet:62)
Autosomal recessive limb-girdle muscular dystrophy type 2I (Orphanet:34515)
Cardiomyopathy, dilated, 1AA with or without left ventricular noncompaction (OMIM:612158)
Cardiomyopathy, dilated, 1D (OMIM:601494)
Cardiomyopathy, dilated, 1EE (OMIM:613252)
Cardiomyopathy, familial hypertrophic, 7 (OMIM:613690)
Cardiomyopathy, familial restrictive, 3 (OMIM:612422)
Cirrhotic cardiomyopathy (Orphanet:57777)
Familial dilated cardiomyopathy with conduction defect due to LMNA mutation (Orphanet:300751)
Hemochromatosis, type 2A (OMIM:602390)
Hemochromatosis, type 2B (OMIM:613313)
His bundle tachycardia (Orphanet:3283)
Left ventricular noncompaction 8 (OMIM:615373)
MELAS (Orphanet:550)
Peripartum cardiomyopathy (Orphanet:563)
Primary hyperoxaluria type 1 (Orphanet:93598)
Tako-Tsubo cardiomyopathy (Orphanet:66529)