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Phenotypic Abnormality (PA): Abnormality of dental enamel

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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)
+ + + + + + + + 8:   Abnormality of head or neck [HP:0000152] <2>(86|104) (97|58|38)
+ + + + + + + 7:   Abnormality of the head [HP:0000234] <6>(85|102) (96|57|38)
+ + + + + + 6:   Abnormality of the face [HP:0000271] <14>(70|85) (82|46|31)
+ + + + + 5:   Abnormality of the mouth [HP:0000153] <2>(37|57) (46|32|22)
+ + + + 4:   Abnormal oral morphology [HP:0031816] <6>(35|53) (44|30|21)
+ + + 3:   Phenotypic abnormality [HP:0000118] <25>
+ + + 3:   Abnormal oral cavity morphology [HP:0000163] <14>(28|43) (36|21|15)
+ + 2:   Abnormality of connective tissue [HP:0003549] <12>(19|27) (19|20|20)
+ + 2:   Abnormality of the skeletal system [HP:0000924] <7>(88|98) (93|54|34)
+ + 2:   Abnormality of the dentition [HP:0000164] <18>(5|11) (8|5|3)
+ 1:   Abnormality of odontoid tissue [HP:3000050] <3>(0|1) (0|1|0)
+ 1:   Abnormality of dental structure [HP:0011061] <8>(2|5) (2|2|0)
0:   Abnormality of dental enamel [HP:0000682] <5>(0|1) (0|1|0)
- 1:   Hypomineralization of enamel [HP:0006285] <2>(0|0) (0|0|0)
- 1:   Hypoplasia of dental enamel [HP:0006297] <2>(0|0) (0|0|0)
- 1:   Amelogenesis imperfecta [HP:0000705](0|0) (0|0|0)
- 1:   Dental enamel pits [HP:0009722](0|0) (0|0|0)
- 1:   Grayish enamel [HP:0000683](0|0) (0|0|0)


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Family

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SCOP termFDR (all)Annotation (direct or inherited)
Laminin-type module0.0005704Direct


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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
  • 0.0009091Direct