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Phenotypic Abnormality (PA): Congenital malformation of the right heart

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Root: HP Hierarchy (human phenotype with 3 sub-ontologies PA, MI, ON)

Shortest distance to current term (+ for parents, - for children) HP term [HP ID] <#Children> (#SF|#FA) #Supra-domain
(Single|Duplex|Triple)
+ + + + 4:   Phenotypic abnormality [HP:0000118] <25>
+ + + 3:   Abnormality of the cardiovascular system [HP:0001626] <5>(60|88) (73|43|30)
+ + 2:   Abnormality of cardiovascular system morphology [HP:0030680] <3>(29|42) (31|19|20)
+ 1:   Abnormal heart morphology [HP:0001627] <16>(20|35) (24|16|20)
0:   Congenital malformation of the right heart [HP:0011723] <3>(0|1) (0|0|0)
- 1:   Double outlet right ventricle [HP:0001719] <8>(0|1) (0|0|0)
- 1:   Hypoplastic right heart [HP:0010954](0|0) (0|0|0)
- 1:   Uhl's anomaly [HP:0011724](0|0) (0|0|0)


Jump to [ Top · Phenotype Hierarchy · Superfamily · Family · Supra-domain ]

Family

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SCOP termFDR (all)Annotation (direct or inherited)
Erythroid transcription factor GATA-10.00007836Direct


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