Abnormality of the left ventricle
Symptom Information:
| Symptom ID: | HPO:0001711 | ||
| Synonyms: |
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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 cardiac ventricle(HPO:0001713) Abnormality of the left ventricle(HPO:0001711) MedDRA: |
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| Database Frequency: | 22 / 7739 | ||
| Resource: |
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) |