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Phenotypic Abnormality (PA): Abnormal myelination

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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)
+ + + 3:   Phenotypic abnormality [HP:0000118] <25>
+ + 2:   Abnormality of the nervous system [HP:0000707] <4>(147|170) (164|102|45)
+ 1:   Abnormality of nervous system morphology [HP:0012639] <5>(70|97) (81|48|16)
0:   Abnormal myelination [HP:0012447] <6>(2|4) (3|0|0)
- 1:   Abnormal peripheral myelination [HP:0003130] <8>(0|2) (1|0|0)
- 1:   Abnormal CNS myelination [HP:0011400] <6>(1|1) (1|0|0)
- 1:   Demyelinating peripheral neuropathy [HP:0007108] <3>(1|0) (1|0|0)
- 1:   Delayed myelination [HP:0012448] <2>(0|0) (0|0|0)
- 1:   Hypermyelinated retinal nerve fibers [HP:0007922](0|0) (0|0|0)
- 1:   Mixed demyelinating and axonal polyneuropathy [HP:0007327](0|0) (0|0|0)


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Superfamily

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SCOP termFDR (all)Annotation (direct or inherited)
NagB/RpiA/CoA transferase-like0.001955Inherited
Ribonuclease H-like0.1743Inherited


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Family

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SCOP termFDR (all)Annotation (direct or inherited)
IF2B-like0Direct
Glutathione S-transferase (GST), C-terminal domain0.0006613Direct
Myotubularin-like phosphatases0.004489Inherited
FHA domain0.005738Inherited


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)
NagB/RpiA/CoA transferase-like0.001114Inherited
SMAD/FHA domain0.01754Inherited
Ribonuclease H-like0.1443Inherited


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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