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Phenotypic Abnormality (PA): Abnormality of the diaphragm

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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)
+ + + 3:   Phenotypic abnormality [HP:0000118] <25>
+ + 2:   Abnormality of the musculature [HP:0003011] <3>(64|83) (70|33|9)
+ 1:   Abnormal skeletal muscle morphology [HP:0011805] <38>(30|36) (35|14|4)
0:   Abnormality of the diaphragm [HP:0000775] <5>(2|3) (2|1|0)
- 1:   Congenital diaphragmatic hernia [HP:0000776] <3>(1|1) (1|1|0)
- 1:   Abnormality of the hemidiaphragms [HP:0040045] <2>(0|0) (0|0|0)
- 1:   Aplasia/Hypoplasia of the diaphragm [HP:0010315] <2>(0|0) (0|0|0)
- 1:   Denervation of the diaphragm [HP:0009109](0|0) (0|0|0)
- 1:   Diaphragmatic eventration [HP:0009110](0|0) (0|0|0)


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Superfamily

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SCOP termFDR (all)Annotation (direct or inherited)
HMG-box0.0001183Direct
ARID-like0.0003664Direct


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Family

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SCOP termFDR (all)Annotation (direct or inherited)
HMG-box0.000037Direct
ARID domain0.0001487Direct
PHD domain0.0009429Direct


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)
HMG-box0.00005486Direct
ARID-like0.0001821Direct

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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
  • 0.0001821Direct


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