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Phenotypic Abnormality (PA): Abnormality of the skull base

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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)
+ + + + 4:   Phenotypic abnormality [HP:0000118] <25>
+ + + + 4:   Abnormality of the skeletal system [HP:0000924] <7>(88|98) (93|55|34)
+ + + 3:   Abnormality of skeletal morphology [HP:0011842] <17>(86|89) (90|52|33)
+ + + 3:   Abnormality of head or neck [HP:0000152] <2>(86|104) (97|58|38)
+ + 2:   Abnormal axial skeleton morphology [HP:0009121] <6>(47|61) (51|30|26)
+ + 2:   Abnormality of the head [HP:0000234] <6>(85|102) (96|57|38)
+ 1:   Abnormal skull morphology [HP:0000929] <14>(25|38) (28|22|20)
0:   Abnormality of the skull base [HP:0002693] <5>(1|1) (2|0|0)
- 1:   Abnormality of the posterior cranial fossa [HP:0000932] <8>(1|1) (2|0|0)
- 1:   Sclerosis of skull base [HP:0002694] <1>(0|0) (0|0|0)
- 1:   Cleft in skull base [HP:0009752](0|0) (0|0|0)
- 1:   Elevated imprint of the transverse sinuses [HP:0000930](0|0) (0|0|0)
- 1:   Thick skull base [HP:0002737](0|0) (0|0|0)


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Superfamily

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SCOP termFDR (all)Annotation (direct or inherited)
ARID-like0.001432Inherited


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Family

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SCOP termFDR (all)Annotation (direct or inherited)
ARID domain0.0007435Direct


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 (Single) FDR (all) Annotation (direct or inherited)
ARID-like0.0007802Direct
WD40 repeat-like0.01233Inherited


Plot distribution on phylogenetic tree for Supra-domains (Single/Individual) annotated by this phenotype term
Plot tree as:   Download Newick format tree:
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