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Phenotypic Abnormality (PA): Mild short stature

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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:   Phenotypic abnormality [HP:0000118] <25>
+ + + + 4:   Growth abnormality [HP:0001507] <6>(29|47) (34|27|21)
+ + + 3:   Growth delay [HP:0001510] <5>(10|14) (13|8|3)
+ + + 3:   Abnormality of body height [HP:0000002] <3>(9|13) (9|7|8)
+ + 2:   Short stature [HP:0004322] <5>(8|11) (8|5|2)
+ 1:   Proportionate short stature [HP:0003508] <3>(2|0) (2|0|0)
0:   Mild short stature [HP:0003502](1|0) (1|0|0)


Jump to [ Top · Phenotype Hierarchy · Superfamily · Family · Supra-domain ]

Superfamily

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SCOP termFDR (all)Annotation (direct or inherited)
FnI-like domain0.00001628Direct


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 domain0.000006994Direct


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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