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Phenotypic Abnormality (PA): Hemihypertrophy

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

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)
+ + 2:   Phenotypic abnormality [HP:0000118] <25>
+ + 2:   Growth abnormality [HP:0001507] <6>(29|48) (34|24|15)
+ 1:   Abnormality of limbs [HP:0040064] <8>(57|64) (59|32|25)
+ 1:   Asymmetric growth [HP:0100555] <4>(0|1) (0|0|0)
0:   Hemihypertrophy [HP:0001528] <2>(0|1) (0|0|0)
- 1:   Hemihypertrophy of lower limb [HP:0100553](0|0) (0|0|0)
- 1:   Hemihypertrophy of upper limb [HP:0100554](0|0) (0|0|0)


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

Family

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SCOP termFDR (all)Annotation (direct or inherited)
G proteins0.0009819Direct


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