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Phenotypic Abnormality (PA): Apraxia

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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:   Abnormality of nervous system physiology [HP:0012638] <26>(101|119) (112|81|39)
+ 1:   Abnormality of higher mental function [HP:0011446] <9>(38|45) (40|24|8)
+ 1:   Abnormality of central motor function [HP:0011442] <10>(22|26) (30|16|7)
0:   Apraxia [HP:0002186] <6>(0|0) (1|0|0)
- 1:   Eyelid apraxia [HP:0000658](0|0) (0|0|0)
- 1:   Gait apraxia [HP:0010521](0|0) (0|0|0)
- 1:   Limb apraxia [HP:0030217](0|0) (0|0|0)
- 1:   Oculomotor apraxia [HP:0000657](0|0) (0|0|0)
- 1:   Oromotor apraxia [HP:0007301](0|0) (0|0|0)
- 1:   Speech apraxia [HP:0011098](0|0) (0|0|0)


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)
HIT-like0.0006413Direct


Plot distribution on phylogenetic tree for Supra-domains (Single/Individual) annotated by this phenotype term
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