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Phenotypic Abnormality (PA): Sensory impairment

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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 the nervous system [HP:0000707] <4>(147|170) (164|102|45)
+ + + 3:   Abnormality of nervous system morphology [HP:0012639] <5>(70|97) (81|48|16)
+ + 2:   Abnormal peripheral nervous system morphology [HP:0000759] <14>(14|17) (17|6|0)
+ 1:   Peripheral neuropathy [HP:0009830] <17>(7|11) (8|4|0)
0:   Sensory impairment [HP:0003474] <7>(1|4) (1|0|0)
- 1:   Abnormality of pain sensation [HP:0010832] <5>(0|0) (0|0|0)
- 1:   Impaired proprioception [HP:0010831] <3>(0|0) (0|0|0)
- 1:   Impaired vibratory sensation [HP:0002495] <3>(0|1) (0|0|0)
- 1:   Distal sensory impairment [HP:0002936] <2>(1|3) (1|0|0)
- 1:   Impaired tactile sensation [HP:0010830] <1>(0|0) (0|0|0)
- 1:   Dissociated sensory loss [HP:0010835](0|0) (0|0|0)
- 1:   Impaired temperature sensation [HP:0010829](0|0) (0|0|0)


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Superfamily

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SCOP termFDR (all)Annotation (direct or inherited)
S15/NS1 RNA-binding domain0.0001485Direct


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Family

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SCOP termFDR (all)Annotation (direct or inherited)
a tRNA synthase domain0.00006642Direct
Myotubularin-like phosphatases0.00006642Direct
Class II aminoacyl-tRNA synthetase (aaRS)-like, catalytic domain0.08218Inherited
Extended AAA-ATPase domain0.1532Inherited


Plot distribution on phylogenetic tree for Superfamily and/or Family domains annotated by this phenotype term
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Jump to [ Top · Phenotype Hierarchy · Superfamily · Family · Supra-domain ]

Supra-domain (including individual superfamily)

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Supra-domain (Single) FDR (all) Annotation (direct or inherited)
S15/NS1 RNA-binding domain0.0000724Direct


Plot distribution on phylogenetic tree for Supra-domains (Single/Individual) annotated by this phenotype term
Plot tree as:   Download Newick format tree:
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