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Phenotypic Abnormality (PA): Mitten deformity

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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:   Phenotypic abnormality [HP:0000118] <25>
+ + + + 4:   Abnormality of limbs [HP:0040064] <8>(57|64) (59|32|25)
+ + + 3:   Abnormality of the upper limb [HP:0002817] <20>(26|29) (30|18|16)
+ + 2:   Abnormality of the hand [HP:0001155] <26>(20|25) (24|16|14)
+ 1:   Abnormal hand morphology [HP:0005922] <11>(2|4) (2|2|4)
0:   Mitten deformity [HP:0004057](0|1) (0|1|1)


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Family

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SCOP termFDR (all)Annotation (direct or inherited)
Laminin-type module0.0000002359Direct


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 (Duplex) in N- to C-terminal order FDR (all) Annotation (direct or inherited)
57196,57196
  • 57196 - EGF/Laminin
  • 57196 - EGF/Laminin
  • 0.0004508Direct

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    Supra-domain (Triple) in N- to C-terminal order FDR (all) Annotation (direct or inherited)
    57196,57196,57196
  • 57196 - EGF/Laminin
  • 57196 - EGF/Laminin
  • 57196 - EGF/Laminin
  • 0.00006776Direct