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Phenotypic Abnormality (PA): Abnormality of upper lip vermillion

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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)
+ + + + + + + + + 9:   Phenotypic abnormality [HP:0000118] <25>
+ + + + + + + + 8:   Abnormality of head or neck [HP:0000152] <2>(87|107) (98|59|37)
+ + + + + + + 7:   Abnormality of the head [HP:0000234] <6>(86|105) (97|58|37)
+ + + + + + 6:   Abnormality of the face [HP:0000271] <14>(72|88) (83|47|30)
+ + + + + 5:   Abnormality of the mouth [HP:0000153] <2>(38|55) (44|30|22)
+ + + + 4:   Abnormal oral morphology [HP:0031816] <6>(36|50) (42|28|21)
+ + + 3:   Abnormal oral cavity morphology [HP:0000163] <14>(29|42) (35|21|15)
+ + 2:   Abnormal lip morphology [HP:0000159] <16>(5|9) (7|3|3)
+ 1:   Abnormality of upper lip [HP:0000177] <7>(4|7) (6|2|3)
0:   Abnormality of upper lip vermillion [HP:0011339] <7>(0|1) (0|1|0)
- 1:   Absent cupid's bow [HP:0010800](0|0) (0|0|0)
- 1:   Everted upper lip vermilion [HP:0010803](0|0) (0|0|0)
- 1:   Exaggerated cupid's bow [HP:0002263](0|0) (0|0|0)
- 1:   Tented upper lip vermilion [HP:0010804](0|0) (0|0|0)
- 1:   Thick upper lip vermilion [HP:0000215](0|0) (0|0|0)
- 1:   Thin upper lip vermilion [HP:0000219](0|1) (0|1|0)
- 1:   U-Shaped upper lip vermilion [HP:0010806](0|0) (0|0|0)


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Family

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SCOP termFDR (all)Annotation (direct or inherited)
SPRY domain0.0008268Direct


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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)
57903,57903
  • 57903 - FYVE/PHD zinc finger
  • 57903 - FYVE/PHD zinc finger
  • 0.00217Inherited