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Phenotypic Abnormality (PA): Follicular hyperkeratosis

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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)
+ + + + + + + 7:   Phenotypic abnormality [HP:0000118] <25>
+ + + + + + 6:   Abnormality of the integument [HP:0001574] <4>(48|69) (59|37|15)
+ + + + + 5:   Abnormality of the skin [HP:0000951] <4>(34|55) (45|36|12)
+ + + + 4:   Abnormality of skin morphology [HP:0011121] <22>(29|49) (40|31|11)
+ + + 3:   Thickened skin [HP:0001072] <4>(3|6) (3|6|2)
+ + 2:   Epidermal thickening [HP:0011368] <9>(3|6) (3|6|2)
+ 1:   Hyperkeratosis [HP:0000962] <21>(2|5) (2|6|2)
0:   Follicular hyperkeratosis [HP:0007502](0|1) (0|1|0)


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Family

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SCOP termFDR (all)Annotation (direct or inherited)
Integrin A (or I) domain0.0004131Direct


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Supra-domain (including individual superfamily)

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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
  • 0.00000002253Direct