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Phenotypic Abnormality (PA): Pes planus

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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 limbs [HP:0040064] <8>(57|64) (59|32|25)
+ + 2:   Abnormality of the lower limb [HP:0002814] <17>(30|31) (33|14|13)
+ 1:   Abnormality of the foot [HP:0001760] <30>(19|21) (19|12|10)
0:   Pes planus [HP:0001763](0|1) (0|0|0)


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Family

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SCOP termFDR (all)Annotation (direct or inherited)
ZZ domain0.0001915Direct


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Supra-domain (including individual superfamily)