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Phenotypic Abnormality (PA): Abnormality of the pharynx

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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 head or neck [HP:0000152] <2>(86|104) (97|58|38)
+ 1:   Abnormality of the head [HP:0000234] <6>(85|102) (96|57|38)
0:   Abnormality of the pharynx [HP:0000600] <8>(0|1) (1|0|0)
- 1:   Abnormality of the nasopharynx [HP:0001739] <3>(0|1) (1|0|0)
- 1:   Abnormal morphology of musculature of pharynx [HP:0430015] <1>(0|0) (0|0|0)
- 1:   Pharyngitis [HP:0025439] <1>(0|0) (0|0|0)
- 1:   Abnormality of hypopharynx [HP:3000053](0|0) (0|0|0)
- 1:   Hypoplasia of the pharynx [HP:0009555](0|0) (0|0|0)
- 1:   Oral-pharyngeal dysphagia [HP:0200136](0|0) (0|0|0)
- 1:   Pharyngeal edema [HP:0011855](0|0) (0|0|0)
- 1:   Posterior pharyngeal cleft [HP:0006783](0|0) (0|0|0)


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Family

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SCOP termFDR (all)Annotation (direct or inherited)
Arylsulfatase0.0002183Direct


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)
Alkaline phosphatase-like0.001513Inherited


Plot distribution on phylogenetic tree for Supra-domains (Single/Individual) annotated by this phenotype term
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