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Phenotypic Abnormality (PA): Narrow face

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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)
+ + + + + + 6:   Phenotypic abnormality [HP:0000118] <25>
+ + + + + 5:   Abnormality of head or neck [HP:0000152] <2>(86|104) (97|58|38)
+ + + + 4:   Abnormality of the head [HP:0000234] <6>(85|102) (96|57|38)
+ + + 3:   Abnormality of the face [HP:0000271] <14>(70|85) (82|46|31)
+ + 2:   Abnormal facial shape [HP:0001999] <16>(6|9) (6|1|0)
+ 1:   Small face [HP:0000274] <2>(2|3) (2|0|0)
0:   Narrow face [HP:0000275](2|3) (2|0|0)


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Superfamily

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SCOP termFDR (all)Annotation (direct or inherited)
Tropomyosin0.0002316Direct
Myosin rod fragments0.0005855Direct


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Family

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SCOP termFDR (all)Annotation (direct or inherited)
Tropomyosin0.0001695Direct
Myosin rod fragments0.0004311Direct
Tandem AAA-ATPase domain0.0005558Direct


Plot distribution on phylogenetic tree for Superfamily and/or Family domains annotated by this phenotype term
Plot tree as:   Download Newick format tree:
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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)
Tropomyosin0.0001125Direct
Myosin rod fragments0.0002992Direct


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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