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Phenotypic Abnormality (PA): Difficulty walking

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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:   Abnormality of the nervous system [HP:0000707] <4>(142|168) (156|103|45)
+ + + + 4:   Phenotypic abnormality [HP:0000118] <25>
+ + + 3:   Abnormality of the musculature [HP:0003011] <3>(64|83) (70|33|9)
+ + + 3:   Abnormality of nervous system physiology [HP:0012638] <26>(101|119) (112|81|39)
+ + 2:   Abnormal muscle physiology [HP:0011804] <12>(44|59) (51|22|5)
+ + 2:   Abnormality of movement [HP:0100022] <19>(23|25) (25|14|3)
+ 1:   Gait disturbance [HP:0001288] <22>(5|4) (8|2|1)
+ 1:   Functional motor deficit [HP:0004302] <7>(1|5) (5|2|0)
0:   Difficulty walking [HP:0002355](0|1) (2|0|0)


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Family

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SCOP termFDR (all)Annotation (direct or inherited)
Clathrin adaptor core protein0.000346Direct


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)
POZ domain0.0006469Direct
HSP20-like chaperones0.0008882Direct


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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