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Phenotypic Abnormality (PA): Squamous cell carcinoma of the skin

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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:   Neoplasm [HP:0002664] <2>(20|21) (23|8|3)
+ + + + 4:   Abnormality of the integument [HP:0001574] <4>(48|69) (59|37|15)
+ + + 3:   Neoplasm by anatomical site [HP:0011793] <24>(18|19) (20|7|2)
+ + + 3:   Abnormality of the skin [HP:0000951] <4>(34|55) (45|36|12)
+ + 2:   Neoplasm of the skin [HP:0008069] <29>(4|5) (4|3|1)
+ 1:   Squamous cell carcinoma [HP:0002860] <2>(1|2) (1|1|1)
0:   Squamous cell carcinoma of the skin [HP:0006739](1|2) (1|1|1)


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Superfamily

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SCOP termFDR (all)Annotation (direct or inherited)
Intermediate filament protein, coiled coil region0.0007439Direct


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Family

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SCOP termFDR (all)Annotation (direct or inherited)
Laminin-type module0.000004454Direct
Intermediate filament protein, coiled coil region0.000226Direct


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)
Intermediate filament protein, coiled coil region0.0003862Direct

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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
  • 0.0008673Direct

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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
  • 0.00005549Direct


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