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Phenotypic Abnormality (PA): Midface retrusion

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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:   Abnormality of head or neck [HP:0000152] <2>(86|104) (97|58|38)
+ + + 3:   Abnormality of the head [HP:0000234] <6>(85|102) (96|57|38)
+ + 2:   Abnormality of the face [HP:0000271] <14>(70|85) (82|46|31)
+ 1:   Abnormality of the midface [HP:0000309] <5>(2|4) (3|2|1)
0:   Midface retrusion [HP:0011800](0|0) (0|1|0)


Jump to [ Top · Phenotype Hierarchy · Superfamily · Family · Supra-domain ]

Supra-domain (including individual superfamily)

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Supra-domain (Duplex) in N- to C-terminal order FDR (all) Annotation (direct or inherited)
117281,117281
  • 117281 - Kelch motif
  • 117281 - Kelch motif
  • 0.0001148Direct