SUPERFAMILY 1.75 HMM library and genome assignments server

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Phenotypic Abnormality (PA): Laryngomalacia

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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 the respiratory system [HP:0002086] <3>(30|35) (38|24|21)
+ + + + 4:   Abnormal respiratory system morphology [HP:0012252] <5>(20|25) (26|18|17)
+ + + 3:   Abnormality of the upper respiratory tract [HP:0002087] <2>(8|9) (8|5|8)
+ + 2:   Abnormality of the larynx [HP:0001600] <3>(5|4) (5|2|1)
+ 1:   Abnormal larynx morphology [HP:0025423] <19>(2|2) (2|0|1)
0:   Laryngomalacia [HP:0001601](1|1) (1|0|0)


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Superfamily

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SCOP termFDR (all)Annotation (direct or inherited)
Intermediate filament protein, coiled coil region0.0001019Direct


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Family

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SCOP termFDR (all)Annotation (direct or inherited)
Intermediate filament protein, coiled coil region0.0001013Direct


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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Supra-domain (including individual superfamily)

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Supra-domain (Single) FDR (all) Annotation (direct or inherited)
Intermediate filament protein, coiled coil region0.00004702Direct


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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