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Phenotypic Abnormality (PA): Amelia

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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:   Abnormality of the skeletal system [HP:0000924] <7>(88|98) (93|54|34)
+ + + 3:   Phenotypic abnormality [HP:0000118] <25>
+ + + 3:   Abnormality of skeletal morphology [HP:0011842] <17>(86|89) (90|52|33)
+ + 2:   Aplasia/hypoplasia involving the skeleton [HP:0009115] <2>(13|11) (15|10|17)
+ + 2:   Abnormality of limbs [HP:0040064] <8>(58|65) (63|33|25)
+ 1:   Aplasia/hypoplasia of the extremities [HP:0009815] <6>(8|9) (10|3|5)
0:   Amelia [HP:0009827] <3>(0|0) (0|0|0)
- 1:   Amelia involving the lower limbs [HP:0009818](0|0) (0|0|0)
- 1:   Amelia involving the upper limbs [HP:0009812](0|0) (0|0|0)
- 1:   Tetraamelia [HP:0003057](0|0) (0|0|0)