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Phenotypic Abnormality (PA): Short neck

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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)
+ + + + + 5:   Abnormality of the skeletal system [HP:0000924] <7>(89|98) (94|51|33)
+ + + + 4:   Abnormality of skeletal morphology [HP:0011842] <18>(87|89) (90|49|32)
+ + + 3:   Abnormal axial skeleton morphology [HP:0009121] <6>(48|61) (53|28|26)
+ + + 3:   Phenotypic abnormality [HP:0000118] <25>
+ + 2:   Abnormality of the vertebral column [HP:0000925] <20>(21|27) (25|11|10)
+ + 2:   Abnormality of head or neck [HP:0000152] <2>(87|107) (98|59|37)
+ 1:   Abnormality of the neck [HP:0000464] <15>(4|8) (5|2|1)
+ 1:   Abnormality of the cervical spine [HP:0003319] <14>(3|5) (4|2|1)
0:   Short neck [HP:0000470](0|2) (1|1|1)


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Family

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SCOP termFDR (all)Annotation (direct or inherited)
Actin/HSP700.0003957Direct
T-box0.0008531Direct


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)
GroEL equatorial domain-like0.0006386Direct

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Supra-domain (Duplex) in N- to C-terminal order FDR (all) Annotation (direct or inherited)
53300,53300
  • 53300 - vWA-like
  • 53300 - vWA-like
  • 0.0006386Direct

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    Supra-domain (Triple) in N- to C-terminal order FDR (all) Annotation (direct or inherited)
    57184,57196,57184
  • 57184 - Growth factor receptor domain
  • 57196 - EGF/Laminin
  • 57184 - Growth factor receptor domain
  • 0.0001566Direct


    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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