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Phenotypic Abnormality (PA): Leukoencephalopathy

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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)
+ + + + + + + 7:   Phenotypic abnormality [HP:0000118] <25>
+ + + + + + 6:   Abnormality of the nervous system [HP:0000707] <4>(147|170) (164|102|45)
+ + + + + 5:   Abnormality of nervous system morphology [HP:0012639] <5>(70|97) (81|48|16)
+ + + + 4:   Morphological abnormality of the central nervous system [HP:0002011] <17>(61|85) (71|41|16)
+ + + 3:   Abnormality of brain morphology [HP:0012443] <13>(44|63) (54|31|14)
+ + 2:   Abnormality of forebrain morphology [HP:0100547] <6>(26|28) (29|15|4)
+ 1:   Abnormality of the cerebrum [HP:0002060] <16>(25|27) (28|15|4)
0:   Leukoencephalopathy [HP:0002352] <5>(1|1) (1|0|0)
- 1:   Abnormality of the periventricular white matter [HP:0002518] <3>(0|0) (0|0|0)
- 1:   Diffuse leukoencephalopathy [HP:0006994](0|0) (0|0|0)
- 1:   Diffuse spongiform leukoencephalopathy [HP:0006943](0|0) (0|0|0)
- 1:   Posterior leukoencephalopathy [HP:0006859](0|0) (0|0|0)
- 1:   Progressive leukoencephalopathy [HP:0006980](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-like0.0001776Direct


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Family

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SCOP termFDR (all)Annotation (direct or inherited)
IF2B-like0Direct


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-like0.00008725Direct


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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