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Phenotypic Abnormality (PA): Coxa vara

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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:   Abnormality of the skeletal system [HP:0000924] <7>(89|98) (94|51|33)
+ + + + + + + 7:   Phenotypic abnormality [HP:0000118] <25>
+ + + + + + + 7:   Abnormality of skeletal morphology [HP:0011842] <18>(87|89) (90|49|32)
+ + + + + + 6:   Abnormal appendicular skeleton morphology [HP:0011844] <4>(35|41) (38|23|23)
+ + + + + + 6:   Abnormality of limbs [HP:0040064] <8>(57|64) (59|32|25)
+ + + + + + 6:   Abnormality of limb bone [HP:0040068] <1>(28|30) (30|18|20)
+ + + + + 5:   Abnormality of limb bone morphology [HP:0002813] <13>(28|30) (30|18|20)
+ + + + + 5:   Abnormality of the lower limb [HP:0002814] <17>(30|31) (33|14|13)
+ + + + 4:   Abnormal lower limb bone morphology [HP:0040069] <10>(10|8) (11|5|6)
+ + + 3:   Abnormality of femur morphology [HP:0002823] <18>(3|4) (4|0|0)
+ + 2:   Abnormality of the femoral neck or head region [HP:0003366] <7>(2|4) (3|0|0)
+ 1:   Abnormality of the femoral neck [HP:0003367] <5>(2|3) (3|0|0)
0:   Coxa vara [HP:0002812](1|0) (1|0|0)


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Superfamily

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SCOP termFDR (all)Annotation (direct or inherited)
FnI-like domain0.00001274Direct


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)
FnI-like domain0.000005673Direct


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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