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Phenotypic Abnormality (PA): Aplasia cutis congenita

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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)
+ + + + + + 6:   Phenotypic abnormality [HP:0000118] <25>
+ + + + + 5:   Abnormality of the integument [HP:0001574] <4>(48|69) (59|37|15)
+ + + + 4:   Abnormality of the skin [HP:0000951] <4>(34|55) (45|36|12)
+ + + 3:   Abnormality of skin morphology [HP:0011121] <22>(29|49) (40|31|11)
+ + 2:   Localized skin lesion [HP:0011355] <29>(12|20) (18|10|6)
+ 1:   Aplasia/Hypoplasia of the skin [HP:0008065] <8>(4|4) (5|2|1)
0:   Aplasia cutis congenita [HP:0001057] <2>(0|1) (0|1|1)
- 1:   Aplasia cutis congenita of scalp [HP:0007385] <2>(0|0) (0|0|0)
- 1:   Aplasia cutis congenita on trunk or limbs [HP:0007589](0|0) (0|0|0)


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Family

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SCOP termFDR (all)Annotation (direct or inherited)
Laminin-type module0.00005147Direct


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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
  • 0.0002223Direct

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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
  • 0.000009568Direct