Hypoplastic left heart
Symptom Information:
Symptom ID: | HPO:0004383 | ||||||||||
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) obsolete Malformation of the heart and great vessels(HPO:0002564) Hypoplastic heart(HPO:0001961) Hypoplastic left heart(HPO:0004383) MedDRA: Cardiac disorders(MedDRA:10007541) Congenital cardiac disorders(MedDRA:10010394) Congenital cardiac structural defects NEC(MedDRA:10010397) Hypoplastic left heart(HPO:0004383) |
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Database Frequency: | 29 / 7739 | ||||||||||
Resource: |
All diseases associated with this symptom:
22q11.2 microduplication syndrome | (Orphanet:1727) |
3C syndrome | (Orphanet:7) |
8p23.1 microdeletion syndrome | (Orphanet:251071) |
Aorta coarctation | (Orphanet:1457) |
Autosomal dominant coarctation of aorta | (Orphanet:1455) |
CHILD syndrome | (Orphanet:139) |
CONGENITAL HEART DEFECTS, MULTIPLE TYPES, 4 | (OMIM:615779) |
Cleft lip/palate - intestinal malrotation - cardiopathy | (Orphanet:2001) |
Congenital alveolar capillary dysplasia | (Orphanet:210122) |
Congenital osteogenesis imperfecta - microcephaly - cataracts | (Orphanet:2772) |
HEART, MALFORMATION OF | (OMIM:140500) |
Histiocytoid cardiomyopathy | (Orphanet:137675) |
Holt-Oram syndrome | (Orphanet:392) |
Holzgreve-Wagner-Rehder syndrome | (Orphanet:2167) |
Hypoplastic left heart syndrome | (Orphanet:2248) |
Hypoplastic left heart syndrome 1 | (OMIM:241550) |
Hypoplastic left heart syndrome 2 | (OMIM:614435) |
Jacobsen syndrome | (Orphanet:2308) |
Left ventricular noncompaction 1 | (OMIM:604169) |
Lethal faciocardiomelic dysplasia | (Orphanet:1972) |
McKusick-Kaufman syndrome | (Orphanet:2473) |
Meacham syndrome | (Orphanet:3097) |
Medeira-Dennis-Donnai syndrome | (Orphanet:2476) |
Okamoto syndrome | (Orphanet:2729) |
PAGOD syndrome | (Orphanet:991) |
Rubinstein-Taybi syndrome due to 16p13.3 microdeletion | (Orphanet:353281) |
Short rib-polydactyly syndrome | (Orphanet:1505) |
Thomas syndrome | (Orphanet:3316) |
Trisomy 17p | (Orphanet:261290) |