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Phenotypic Abnormality (PA): Aplasia involving bones of the upper limbs

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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:   Abnormality of the skeletal system [HP:0000924] <7>(88|98) (93|55|34)
+ + + + + 5:   Abnormality of skeletal morphology [HP:0011842] <17>(86|89) (90|52|33)
+ + + + 4:   Abnormality of limb bone [HP:0040068] <1>(29|32) (33|18|20)
+ + + + 4:   Phenotypic abnormality [HP:0000118] <25>
+ + + + 4:   Abnormal appendicular skeleton morphology [HP:0011844] <4>(35|43) (39|23|23)
+ + + + 4:   Aplasia/hypoplasia involving the skeleton [HP:0009115] <2>(13|12) (15|10|17)
+ + + 3:   Abnormality of limb bone morphology [HP:0002813] <13>(29|32) (32|18|20)
+ + + 3:   Abnormality of limbs [HP:0040064] <8>(58|66) (63|33|25)
+ + + 3:   Aplasia/hypoplasia of the extremities [HP:0009815] <6>(8|10) (10|3|5)
+ + 2:   Aplasia/hypoplasia involving bones of the extremities [HP:0045060] <3>(7|9) (9|3|5)
+ + 2:   Abnormality of the upper limb [HP:0002817] <20>(29|35) (35|17|16)
+ 1:   Aplasia/hypoplasia involving bones of the upper limbs [HP:0006496] <8>(3|8) (6|2|4)
+ 1:   Aplasia involving bones of the extremities [HP:0009825] <2>(0|1) (0|0|0)
0:   Aplasia involving bones of the upper limbs [HP:0009823] <1>(0|1) (0|0|0)
- 1:   Aplasia of the phalanges of the hand [HP:0009802] <3>(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 domains0.0002274Direct


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