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Phenotypic Abnormality (PA): Oral mucosal blisters

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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:   Abnormality of head or neck [HP:0000152] <2>(86|104) (97|58|38)
+ + + + + + 6:   Abnormality of the head [HP:0000234] <6>(85|102) (96|57|38)
+ + + + + 5:   Phenotypic abnormality [HP:0000118] <25>
+ + + + + 5:   Abnormality of the face [HP:0000271] <14>(70|85) (82|46|31)
+ + + + 4:   Abnormality of the integument [HP:0001574] <4>(48|69) (59|37|15)
+ + + + 4:   Abnormality of the mouth [HP:0000153] <2>(37|57) (46|32|22)
+ + + 3:   Abnormal oral morphology [HP:0031816] <6>(35|53) (44|30|21)
+ + + 3:   Abnormality of the skin [HP:0000951] <4>(34|55) (45|36|12)
+ + 2:   Abnormality of skin morphology [HP:0011121] <22>(29|49) (40|31|11)
+ + 2:   Abnormal oral cavity morphology [HP:0000163] <14>(28|43) (36|21|15)
+ 1:   Abnormal oral mucosa morphology [HP:0011830] <15>(10|16) (13|8|3)
+ 1:   Abnormal blistering of the skin [HP:0008066] <4>(3|2) (3|3|1)
0:   Oral mucosal blisters [HP:0200097](0|1) (0|1|1)


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Family

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SCOP termFDR (all)Annotation (direct or inherited)
Laminin-type module0.000002358Direct


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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)
57196,57196
  • 57196 - EGF/Laminin
  • 57196 - EGF/Laminin
  • 0.0002994Direct

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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
  • 0.0002825Direct