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Phenotypic Abnormality (PA): Protruding ear

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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)
+ + + + + 5:   Phenotypic abnormality [HP:0000118] <25>
+ + + + 4:   Abnormality of the ear [HP:0000598] <2>(18|32) (22|13|10)
+ + + 3:   Abnormal ear morphology [HP:0031703] <5>(15|26) (18|11|10)
+ + 2:   Abnormality of the outer ear [HP:0000356] <14>(6|7) (7|3|1)
+ 1:   Abnormality of the pinna [HP:0000377] <28>(3|3) (3|2|0)
0:   Protruding ear [HP:0000411](1|1) (1|1|0)


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Superfamily

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SCOP termFDR (all)Annotation (direct or inherited)
MIR domain0.0007825Direct


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Family

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SCOP termFDR (all)Annotation (direct or inherited)
MIR domain0.0004907Direct


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)
MIR domain0.0004182Direct

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Supra-domain (Duplex) in N- to C-terminal order FDR (all) Annotation (direct or inherited)
53300,53300
  • 53300 - vWA-like
  • 53300 - vWA-like
  • 0.00007394Direct


    Plot distribution on phylogenetic tree for Supra-domains (Single/Individual) annotated by this phenotype term
    Plot tree as:   Download Newick format tree:
    (show help)