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Phenotypic Abnormality (PA): Demyelinating peripheral neuropathy

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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>
+ + + 3:   Abnormality of the nervous system [HP:0000707] <4>(142|168) (156|103|45)
+ + 2:   Abnormal peripheral nervous system morphology [HP:0000759] <14>(14|17) (18|6|0)
+ + 2:   Abnormality of nervous system morphology [HP:0012639] <5>(69|97) (79|52|16)
+ 1:   Peripheral neuropathy [HP:0009830] <17>(7|11) (9|4|0)
+ 1:   Abnormal myelination [HP:0012447] <6>(3|5) (4|1|0)
0:   Demyelinating peripheral neuropathy [HP:0007108] <3>(1|0) (1|0|0)
- 1:   Acute demyelinating polyneuropathy [HP:0007131](0|0) (0|0|0)
- 1:   Demyelinating motor neuropathy [HP:0007220](0|0) (0|0|0)
- 1:   Demyelinating sensory neuropathy [HP:0011402](0|0) (0|0|0)


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Superfamily

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SCOP termFDR (all)Annotation (direct or inherited)
Ribonuclease H-like0.00005167Direct


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)
Ribonuclease H-like0.00002318Direct


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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