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Phenotypic Abnormality (PA): Bilateral single transverse palmar creases

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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)
+ + + + + + + + + 9:   Phenotypic abnormality [HP:0000118] <25>
+ + + + + + + + 8:   Abnormality of limbs [HP:0040064] <8>(57|64) (59|32|25)
+ + + + + + + + 8:   Abnormality of the integument [HP:0001574] <4>(46|69) (58|36|15)
+ + + + + + + 7:   Abnormality of the skin [HP:0000951] <4>(33|53) (45|35|12)
+ + + + + + + 7:   Abnormality of the upper limb [HP:0002817] <20>(26|29) (30|18|16)
+ + + + + + 6:   Abnormality of the hand [HP:0001155] <26>(20|25) (24|16|14)
+ + + + + + 6:   Abnormality of skin morphology [HP:0011121] <22>(28|47) (40|30|11)
+ + + + + 5:   Abnormality of the palm [HP:0100871] <6>(6|7) (8|2|1)
+ + + + + 5:   Regional abnormality of skin [HP:0011356] <11>(7|9) (9|5|1)
+ + + + 4:   Abnormal dermatoglyphics [HP:0007477] <5>(2|3) (3|1|0)
+ + + + 4:   Abnormality of the skin of the palm [HP:0040211] <9>(4|5) (6|2|1)
+ + + 3:   Abnormal palmar dermatoglyphics [HP:0001018] <8>(1|2) (3|0|0)
+ + 2:   Abnormality of the palmar creases [HP:0010490] <7>(1|2) (3|0|0)
+ 1:   Single transverse palmar crease [HP:0000954] <1>(1|2) (3|0|0)
0:   Bilateral single transverse palmar creases [HP:0007598](1|1) (1|0|0)


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Superfamily

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SCOP termFDR (all)Annotation (direct or inherited)
ARID-like0.00002797Direct


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Family

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SCOP termFDR (all)Annotation (direct or inherited)
ARID domain0.00001232Direct


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-like0.0000128Direct


Plot distribution on phylogenetic tree for Supra-domains (Single/Individual) annotated by this phenotype term
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