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Phenotypic Abnormality (PA): Abnormality of odontoid tissue

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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)
+ + 2:   Phenotypic abnormality [HP:0000118] <25>
+ 1:   Abnormality of the skeletal system [HP:0000924] <7>(88|98) (93|55|34)
+ 1:   Abnormality of connective tissue [HP:0003549] <12>(19|27) (19|20|20)
0:   Abnormality of odontoid tissue [HP:3000050] <3>(0|1) (0|1|0)
- 1:   Abnormality of dental enamel [HP:0000682] <5>(0|1) (0|1|0)
- 1:   Dentinogenesis imperfecta [HP:0000703] <3>(0|0) (0|0|0)
- 1:   Abnormality of the cementum [HP:0100717](0|0) (0|0|0)


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

Family

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SCOP termFDR (all)Annotation (direct or inherited)
Laminin-type module0.002015Inherited


Plot distribution on phylogenetic tree for Superfamily and/or Family domains annotated by this phenotype term
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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)
57196,57196
  • 57196 - EGF/Laminin
  • 57196 - EGF/Laminin
  • 0.00498Inherited