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Phenotypic Abnormality (PA): Aplasia involving bones of the extremities

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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>
+ + + + 4:   Abnormality of skeletal morphology [HP:0011842] <18>(87|89) (90|49|32)
+ + + + 4:   Abnormality of the skeletal system [HP:0000924] <7>(89|98) (94|51|33)
+ + + 3:   Abnormal appendicular skeleton morphology [HP:0011844] <4>(35|41) (38|23|23)
+ + + 3:   Aplasia/hypoplasia involving the skeleton [HP:0009115] <2>(13|11) (13|10|17)
+ + + 3:   Abnormality of limbs [HP:0040064] <8>(57|64) (59|32|25)
+ + + 3:   Abnormality of limb bone [HP:0040068] <1>(28|30) (30|18|20)
+ + 2:   Abnormality of limb bone morphology [HP:0002813] <13>(28|30) (30|18|20)
+ + 2:   Aplasia/hypoplasia of the extremities [HP:0009815] <6>(8|9) (9|3|5)
+ 1:   Aplasia/hypoplasia involving bones of the extremities [HP:0045060] <3>(7|8) (8|3|5)
0:   Aplasia involving bones of the extremities [HP:0009825] <2>(0|1) (0|0|0)
- 1:   Aplasia involving bones of the lower limbs [HP:0009817] <2>(0|0) (0|0|0)
- 1:   Aplasia involving bones of the upper limbs [HP:0009823] <1>(0|1) (0|0|0)


Jump to [ Top · Phenotype Hierarchy · Superfamily · Family · Supra-domain ]

Family

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SCOP termFDR (all)Annotation (direct or inherited)
I set domains0.0004058Direct


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