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Phenotypic Abnormality (PA): Congenital diaphragmatic hernia

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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>
+ + + 3:   Abnormality of the musculature [HP:0003011] <3>(64|83) (70|33|9)
+ + 2:   Abnormal skeletal muscle morphology [HP:0011805] <38>(30|36) (35|14|4)
+ + 2:   Abnormality of connective tissue [HP:0003549] <12>(19|27) (19|20|20)
+ 1:   Abnormality of the diaphragm [HP:0000775] <5>(2|3) (2|1|0)
+ 1:   Hernia [HP:0100790] <4>(5|7) (5|5|7)
0:   Congenital diaphragmatic hernia [HP:0000776] <3>(1|1) (1|1|0)
- 1:   Central diaphragmatic hernia [HP:0025195](0|0) (0|0|0)
- 1:   Morgagni diaphragmatic hernia [HP:0025194](0|0) (0|0|0)
- 1:   Posterolateral diaphragmatic hernia [HP:0025193](0|0) (0|0|0)


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Superfamily

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SCOP termFDR (all)Annotation (direct or inherited)
HMG-box0.00004307Direct


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Family

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SCOP termFDR (all)Annotation (direct or inherited)
HMG-box0.00001192Direct


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-box0.00001915Direct

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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
  • 0.00002026Direct


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