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Phenotypic Abnormality (PA): Abnormality of abdominal situs

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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)
+ + + 3:   Phenotypic abnormality [HP:0000118] <25>
+ + 2:   Abnormality of the digestive system [HP:0025031] <6>(67|77) (77|47|25)
+ + 2:   Growth abnormality [HP:0001507] <6>(29|47) (34|27|21)
+ 1:   Heterotaxy [HP:0030853] <2>(0|0) (0|0|0)
+ 1:   Abnormality of the abdominal organs [HP:0002012] <6>(27|27) (30|14|4)
0:   Abnormality of abdominal situs [HP:0011620] <2>(0|0) (0|0|0)
- 1:   Abdominal situs ambiguus [HP:0031565](0|0) (0|0|0)
- 1:   Abdominal situs inversus [HP:0003363](0|0) (0|0|0)