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Phenotypic Abnormality (PA): Single ventricle

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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)
+ + + + + 5:   Phenotypic abnormality [HP:0000118] <25>
+ + + + 4:   Abnormality of the cardiovascular system [HP:0001626] <5>(60|88) (73|43|30)
+ + + 3:   Abnormality of cardiovascular system morphology [HP:0030680] <3>(29|42) (31|19|20)
+ + 2:   Abnormal heart morphology [HP:0001627] <16>(20|35) (24|16|20)
+ 1:   Abnormal cardiac ventricle morphology [HP:0001713] <9>(5|9) (5|5|10)
0:   Single ventricle [HP:0001750] <4>(0|0) (0|0|0)
- 1:   Double inlet to single ventricle of indeterminate morphology [HP:0011557] <2>(0|0) (0|0|0)
- 1:   Double inlet left ventricle [HP:0011555](0|0) (0|0|0)
- 1:   Double inlet right ventricle [HP:0011556](0|0) (0|0|0)
- 1:   Single ventricle of indeterminate morphology [HP:0011680](0|0) (0|0|0)