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Phenotypic Abnormality (PA): Abnormal dermatoglyphics

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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:   Abnormality of the integument [HP:0001574] <4>(46|69) (58|36|15)
+ + + 3:   Abnormality of the skin [HP:0000951] <4>(33|53) (45|35|12)
+ + 2:   Abnormality of skin morphology [HP:0011121] <22>(28|47) (40|30|11)
+ 1:   Regional abnormality of skin [HP:0011356] <11>(7|9) (9|5|1)
0:   Abnormal dermatoglyphics [HP:0007477] <5>(2|3) (3|1|0)
- 1:   Abnormal palmar dermatoglyphics [HP:0001018] <8>(1|2) (3|0|0)
- 1:   Abnormal plantar dermatoglyphics [HP:0010506](0|0) (0|0|0)
- 1:   Adermatoglyphia [HP:0007455](0|0) (0|0|0)
- 1:   Interdigital loops [HP:0100888](0|0) (0|0|0)
- 1:   Palmoplantar cutis gyrata [HP:0007469](0|0) (0|0|0)


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Superfamily

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SCOP termFDR (all)Annotation (direct or inherited)
Bromodomain0.0009978Direct
ARID-like0.001174Inherited


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Family

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SCOP termFDR (all)Annotation (direct or inherited)
Bromodomain0.0005706Direct
PHD domain0.0006174Direct
ARID domain0.0006768Direct


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)
Bromodomain0.0005442Direct
ARID-like0.0006458Direct
SET domain0.1498Inherited

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Supra-domain (Duplex) in N- to C-terminal order FDR (all) Annotation (direct or inherited)
57903,57903
  • 57903 - FYVE/PHD zinc finger
  • 57903 - FYVE/PHD zinc finger
  • 0.0006458Direct


    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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