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Phenotypic Abnormality (PA): Hypoplasia of the maxilla

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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)
+ + + + + + + 7:   Phenotypic abnormality [HP:0000118] <25>
+ + + + + + + 7:   Abnormality of the skeletal system [HP:0000924] <7>(88|98) (93|55|34)
+ + + + + + 6:   Abnormality of skeletal morphology [HP:0011842] <17>(86|89) (90|52|33)
+ + + + + + 6:   Abnormality of head or neck [HP:0000152] <2>(86|104) (97|58|38)
+ + + + + 5:   Abnormal axial skeleton morphology [HP:0009121] <6>(47|61) (51|30|26)
+ + + + + 5:   Abnormality of the head [HP:0000234] <6>(85|102) (96|57|38)
+ + + + 4:   Abnormal skull morphology [HP:0000929] <14>(25|38) (28|22|20)
+ + + 3:   Abnormality of facial skeleton [HP:0011821] <14>(4|4) (5|6|9)
+ + 2:   Abnormal jaw morphology [HP:0030791] <4>(3|2) (3|5|8)
+ 1:   Abnormality of the maxilla [HP:0000326] <9>(0|1) (0|1|1)
0:   Hypoplasia of the maxilla [HP:0000327] <3>(0|1) (0|1|1)
- 1:   Hypoplasia of maxilla relative to mandible [HP:0410218](0|0) (0|0|0)
- 1:   Hypoplasia of the anterior nasal spine [HP:0010666](0|0) (0|0|0)
- 1:   Maxillozygomatic hypoplasia [HP:0005439](0|0) (0|0|0)


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Family

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SCOP termFDR (all)Annotation (direct or inherited)
Cadherin0.0009026Direct


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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)
49313,49313
  • 49313 - Cadherin-like
  • 49313 - Cadherin-like
  • 0.0007099Direct

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    Supra-domain (Triple) in N- to C-terminal order FDR (all) Annotation (direct or inherited)
    49313,49313,49313
  • 49313 - Cadherin-like
  • 49313 - Cadherin-like
  • 49313 - Cadherin-like
  • 0.0007099Direct