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Phenotypic Abnormality (PA): Impaired vibration sensation in the lower limbs

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

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)
+ + + + + + + 7:   Phenotypic abnormality [HP:0000118] <25>
+ + + + + + 6:   Abnormality of the nervous system [HP:0000707] <4>(142|168) (156|103|45)
+ + + + + 5:   Abnormality of nervous system morphology [HP:0012639] <5>(69|97) (79|52|16)
+ + + + 4:   Abnormal peripheral nervous system morphology [HP:0000759] <14>(14|17) (18|6|0)
+ + + 3:   Peripheral neuropathy [HP:0009830] <17>(7|11) (9|4|0)
+ + 2:   Sensory impairment [HP:0003474] <7>(3|4) (4|0|0)
+ 1:   Impaired vibratory sensation [HP:0002495] <3>(0|1) (0|0|0)
0:   Impaired vibration sensation in the lower limbs [HP:0002166] <1>(0|1) (0|0|0)
- 1:   Impaired vibration sensation at ankles [HP:0006938](0|0) (0|0|0)


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

Family

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SCOP termFDR (all)Annotation (direct or inherited)
Extended AAA-ATPase domain0.0002628Direct


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