SUPERFAMILY 1.75 HMM library and genome assignments server

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Phenotypic Abnormality (PA): Bifid tongue

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Jump to [ Top · Phenotype Hierarchy · Superfamily · Family · Supra-domain ]

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)
+ + + + + + + + + 9:   Phenotypic abnormality [HP:0000118] <25>
+ + + + + + + + 8:   Abnormality of head or neck [HP:0000152] <2>(86|104) (97|58|38)
+ + + + + + + 7:   Abnormality of the head [HP:0000234] <6>(85|102) (96|57|38)
+ + + + + + 6:   Abnormality of the face [HP:0000271] <14>(70|85) (82|46|31)
+ + + + + 5:   Abnormality of the mouth [HP:0000153] <2>(37|57) (46|32|22)
+ + + + 4:   Abnormal oral morphology [HP:0031816] <6>(35|53) (44|30|21)
+ + + 3:   Abnormal oral cavity morphology [HP:0000163] <14>(28|43) (36|21|15)
+ + 2:   Abnormality of the tongue [HP:0000157] <4>(1|3) (1|1|1)
+ 1:   Abnormal tongue morphology [HP:0030809] <22>(0|2) (0|1|1)
0:   Bifid tongue [HP:0010297](0|1) (0|0|0)


Jump to [ Top · Phenotype Hierarchy · Superfamily · Family · Supra-domain ]

Family

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SCOP termFDR (all)Annotation (direct or inherited)
PDZ domain0.00002874Direct


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