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Phenotypic Abnormality (PA): Abnormal gastrointestinal motility

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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 digestive system [HP:0025031] <6>(63|72) (76|45|24)
+ + 2:   Abnormality of digestive system physiology [HP:0025032] <5>(26|31) (35|16|2)
+ + 2:   Abnormality of the gastrointestinal tract [HP:0011024] <3>(22|26) (28|11|3)
+ 1:   Functional abnormality of the gastrointestinal tract [HP:0012719] <11>(9|11) (14|2|0)
0:   Abnormal gastrointestinal motility [HP:0030895] <2>(2|2) (2|1|0)
- 1:   Gastrointestinal dysmotility [HP:0002579] <4>(1|1) (1|1|0)
- 1:   Abnormal gastrointestinal transit time [HP:0030896] <2>(0|0) (0|0|0)


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Superfamily

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SCOP termFDR (all)Annotation (direct or inherited)
Ran binding protein zinc finger-like0.00008411Direct
Actin-like ATPase domain0.002972Inherited


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Family

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SCOP termFDR (all)Annotation (direct or inherited)
Ran binding protein zinc finger-like0.00004291Direct
Actin/HSP700.0004379Direct


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)
Ran binding protein zinc finger-like0.00004013Direct
Actin-like ATPase domain0.001756Inherited

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Supra-domain (Duplex) in N- to C-terminal order FDR (all) Annotation (direct or inherited)
53067,53067
  • 53067 - Actin-like ATPase domain
  • 53067 - Actin-like ATPase domain
  • 0.001756Inherited


    Plot distribution on phylogenetic tree for Supra-domains (Single/Individual) annotated by this phenotype term
    Plot tree as:   Download Newick format tree:
    (show help)