Hypoplastic left heart

Symptom Information:

Symptom ID: HPO:0004383
Synonyms:
Left ventricle hypoplasia [Orphanet:34300]
Left ventricular hypoplasia (disorder) [Orphanet:34300]
Hypoplastic left heart syndrome (disorder) [Orphanet:34300]
Left ventricular hypoplasia [Orphanet:34300]
Hypoplastic Left Heart Syndrome [Orphanet:34300]
Hypoplastic left heart [OMIM:Hypoplastic left heart]
Hypoplastic left heart/ventricle [Orphanet:34300]
Hypoplastic left heart syndrome [Orphanet:34300]
Hypoplastic left heart syndrome [MedDRA:10021076]
Hypoplastic left heart syndrome [OMIM:Hypoplastic left heart syndrome]
Quality:
Cross references:
HPO:0001961 "Hypoplastic heart" [Orphanet:34300]
Orphanet:34300 "Hypoplastic left heart/ventricle" [Orphanet:34300]
OMIM: "Hypoplastic left heart" [OMIM:Hypoplastic left heart]
OMIM: "Hypoplastic left heart syndrome" [OMIM:Hypoplastic left heart syndrome]
UMLS:C0344906 "Left ventricular hypoplasia" [Orphanet:34300]
UMLS:C0152101 "Hypoplastic Left Heart Syndrome" [Orphanet:34300]
Is a (Direct Parents):
MedDRA Congenital cardiac structural defects NEC
Orphanet obsolete Malformation of the heart and great vessels
HPO         Hypoplastic heart
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)
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)