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Phenotypic Abnormality (PA): Limitation of movement at ankles

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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 limbs [HP:0040064] <8>(58|65) (63|33|25)
+ + + + 4:   Abnormality of the skeletal system [HP:0000924] <7>(88|98) (93|54|34)
+ + + + 4:   Abnormality of skeletal morphology [HP:0011842] <17>(86|89) (90|52|33)
+ + + 3:   Abnormality of the lower limb [HP:0002814] <17>(31|34) (35|15|13)
+ + + 3:   Abnormality of skeletal physiology [HP:0011843] <8>(17|23) (17|15|15)
+ + + 3:   Abnormal joint morphology [HP:0001367] <18>(19|23) (20|9|2)
+ + 2:   Abnormality of joint mobility [HP:0011729] <6>(16|21) (16|15|15)
+ + 2:   Abnormality of lower limb joint [HP:0100491] <5>(10|13) (11|2|1)
+ 1:   Limitation of joint mobility [HP:0001376] <13>(2|2) (2|7|12)
+ 1:   Abnormality of the ankles [HP:0003028] <9>(2|1) (2|1|0)
0:   Limitation of movement at ankles [HP:0010505](0|0) (0|0|0)