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Phenotypic Abnormality (PA): Retrognathia

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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)
+ + + + + + + 7:   Phenotypic abnormality [HP:0000118] <25>
+ + + + + + + 7:   Abnormality of the skeletal system [HP:0000924] <7>(88|98) (93|54|34)
+ + + + + + 6:   Abnormality of head or neck [HP:0000152] <2>(86|104) (97|58|38)
+ + + + + + 6:   Abnormality of skeletal morphology [HP:0011842] <17>(86|89) (90|52|33)
+ + + + + 5:   Abnormality of the head [HP:0000234] <6>(85|102) (96|57|38)
+ + + + + 5:   Abnormal axial skeleton morphology [HP:0009121] <6>(47|61) (51|30|26)
+ + + + 4:   Abnormal skull morphology [HP:0000929] <14>(25|38) (28|22|20)
+ + + 3:   Abnormality of facial skeleton [HP:0011821] <14>(4|4) (5|6|9)
+ + 2:   Abnormal jaw morphology [HP:0030791] <4>(3|2) (3|5|8)
+ 1:   Abnormality of the mandible [HP:0000277] <20>(3|1) (3|3|7)
0:   Retrognathia [HP:0000278] <1>(2|0) (2|0|0)
- 1:   Microretrognathia [HP:0000308](0|0) (0|0|0)


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Superfamily

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SCOP termFDR (all)Annotation (direct or inherited)
"Winged helix" DNA-binding domain0.00003961Direct
Acyl-CoA N-acyltransferases (Nat)0.0005641Direct


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)
"Winged helix" DNA-binding domain0.00001761Direct
Acyl-CoA N-acyltransferases (Nat)0.0002876Direct


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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