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Phenotypic Abnormality (PA): Hyperlordosis

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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)
+ + + + + + 6:   Phenotypic abnormality [HP:0000118] <25>
+ + + + + 5:   Abnormality of the skeletal system [HP:0000924] <7>(89|98) (94|51|33)
+ + + + 4:   Abnormality of skeletal morphology [HP:0011842] <18>(87|89) (90|49|32)
+ + + 3:   Abnormal axial skeleton morphology [HP:0009121] <6>(48|61) (53|28|26)
+ + 2:   Abnormality of the vertebral column [HP:0000925] <20>(21|27) (25|11|10)
+ 1:   Abnormality of the curvature of the vertebral column [HP:0010674] <6>(12|15) (13|7|4)
0:   Hyperlordosis [HP:0003307] <1>(1|1) (1|0|0)
- 1:   Lumbar hyperlordosis [HP:0002938](1|1) (1|0|0)


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Superfamily

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SCOP termFDR (all)Annotation (direct or inherited)
MIR domain0.001434Inherited


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Family

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SCOP termFDR (all)Annotation (direct or inherited)
MIR domain0.0008827Direct


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)
MIR domain0.0008005Direct


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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