Abnormality of the left ventricle

Symptom Information:

Symptom ID: HPO:0001711
Left ventricular abnormality [HPO:0001711]
Cross references:
Is a (Direct Parents):
HPO         Abnormality of cardiac ventricle
Is a (Whole tree): HPO:
    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)
Database Frequency: 22 / 7739

All diseases associated with this symptom:

1p36 deletion syndrome (Orphanet:1606)
Alström syndrome (Orphanet:64)
Arrhythmogenic right ventricular dysplasia, familial, 8 (OMIM:607450)
Arrhythmogenic right ventricular dysplasia, familial, 9 (OMIM:609040)
Atrial fibrillation, familial, 10 (OMIM:614022)
Atrial fibrillation, familial, 3 (OMIM:607554)
Cardiomyopathy, dilated, 1M (OMIM:607482)
Cardiomyopathy, dilated, 1S (OMIM:613426)
Cardiomyopathy, dilated, 2A (OMIM:611880)
Cardiomyopathy, dilated, 3B (OMIM:302045)
Cardiomyopathy, familial restrictive, 1 (OMIM:115210)
Familial isolated dilated cardiomyopathy (Orphanet:154)
Familial isolated restrictive cardiomyopathy (Orphanet:75249)
Incessant infant ventricular tachycardia (Orphanet:45453)
Left ventricular noncompaction (Orphanet:54260)
Long chain 3-hydroxyacyl-CoA dehydrogenase deficiency (Orphanet:5)
Moyamoya disease - short stature - facial dysmorphism - hypergonadotropic hypogonadism (Orphanet:280679)
Mulibrey nanism (Orphanet:2576)
Symptomatic form of muscular dystrophy of Duchenne and Becker in female carriers (Orphanet:206546)
Systemic sclerosis (Orphanet:90291)
Tako-Tsubo cardiomyopathy (Orphanet:66529)
Transaldolase deficiency (Orphanet:101028)