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Phenotypic Abnormality (PA): Encephalocele

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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:   Abnormality of the skeletal system [HP:0000924] <7>(88|98) (93|54|34)
+ + + + 4:   Phenotypic abnormality [HP:0000118] <25>
+ + + + 4:   Abnormality of skeletal morphology [HP:0011842] <17>(86|89) (90|52|33)
+ + + + 4:   Abnormality of head or neck [HP:0000152] <2>(86|104) (97|58|38)
+ + + 3:   Abnormality of the nervous system [HP:0000707] <4>(142|168) (156|103|45)
+ + + 3:   Abnormality of the head [HP:0000234] <6>(85|102) (96|57|38)
+ + + 3:   Abnormal axial skeleton morphology [HP:0009121] <6>(47|61) (51|30|26)
+ + 2:   Abnormality of nervous system morphology [HP:0012639] <5>(69|97) (79|52|16)
+ + 2:   Abnormal skull morphology [HP:0000929] <14>(25|38) (28|22|20)
+ 1:   Morphological abnormality of the central nervous system [HP:0002011] <17>(60|85) (69|44|16)
+ 1:   Cephalocele [HP:0011815] <2>(0|1) (0|1|1)
0:   Encephalocele [HP:0002084] <9>(0|1) (0|1|1)
- 1:   Basal encephalocele [HP:0011817] <1>(0|0) (0|0|0)
- 1:   Frontal encephalocele [HP:0007330] <1>(0|0) (0|0|0)
- 1:   Anterior basal encephalocele [HP:0006992](0|0) (0|0|0)
- 1:   Anterior encephalocele [HP:0007035](0|0) (0|0|0)
- 1:   Cranium bifidum occultum [HP:0004423](0|0) (0|0|0)
- 1:   Meningoencephalocele [HP:0006888](0|0) (0|0|0)
- 1:   Occipital encephalocele [HP:0002085](0|0) (0|0|0)
- 1:   Orbital encephalocele [HP:0007115](0|0) (0|0|0)
- 1:   Parietal encephalocele [HP:0011816](0|0) (0|0|0)


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Family

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SCOP termFDR (all)Annotation (direct or inherited)
Homeodomain0.0006508Direct


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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)
57196,57184
  • 57196 - EGF/Laminin
  • 57184 - Growth factor receptor domain
  • 0.0009167Direct

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    Supra-domain (Triple) in N- to C-terminal order FDR (all) Annotation (direct or inherited)
    57196,57196,57184
  • 57196 - EGF/Laminin
  • 57196 - EGF/Laminin
  • 57184 - Growth factor receptor domain
  • 0.0009167Direct