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Phenotypic Abnormality (PA): Abnormal tongue morphology

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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)
+ + + + + + + + 8:   Phenotypic abnormality [HP:0000118] <25>
+ + + + + + + 7:   Abnormality of head or neck [HP:0000152] <2>(86|104) (97|58|38)
+ + + + + + 6:   Abnormality of the head [HP:0000234] <6>(85|102) (96|57|38)
+ + + + + 5:   Abnormality of the face [HP:0000271] <14>(70|85) (82|46|31)
+ + + + 4:   Abnormality of the mouth [HP:0000153] <2>(37|57) (46|32|22)
+ + + 3:   Abnormal oral morphology [HP:0031816] <6>(35|53) (44|30|21)
+ + 2:   Abnormal oral cavity morphology [HP:0000163] <14>(28|43) (36|21|15)
+ 1:   Abnormality of the tongue [HP:0000157] <4>(1|3) (1|1|1)
0:   Abnormal tongue morphology [HP:0030809] <22>(0|2) (0|1|1)
- 1:   Abnormality of the tongue muscle [HP:0040173] <2>(0|0) (0|0|0)
- 1:   Aplasia/Hypoplasia of the tongue [HP:0010295] <2>(0|0) (0|0|0)
- 1:   Macroglossia [HP:0000158] <2>(0|0) (0|0|0)
- 1:   Furrowed tongue [HP:0000221] <1>(0|0) (0|0|0)
- 1:   Abnormal hyoglossus muscle morphology [HP:3000051](0|0) (0|0|0)
- 1:   Abnormal lingual artery morphology [HP:3000074](0|0) (0|0|0)
- 1:   Abnormality of lingual tonsil [HP:3000076](0|0) (0|0|0)
- 1:   Ankyloglossia [HP:0010296](0|1) (0|1|1)
- 1:   Bifid tongue [HP:0010297](0|1) (0|0|0)
- 1:   Duplicated tongue [HP:0040294](0|0) (0|0|0)
- 1:   Geographic tongue [HP:0025252](0|0) (0|0|0)
- 1:   Glossitis [HP:0000206](0|0) (0|0|0)
- 1:   Glossoptosis [HP:0000162](0|0) (0|0|0)
- 1:   Lobulated tongue [HP:0000180](0|0) (0|0|0)
- 1:   Posteriorly placed tongue [HP:0009087](0|0) (0|0|0)
- 1:   Protruding tongue [HP:0010808](0|0) (0|0|0)
- 1:   Smooth tongue [HP:0010298](0|0) (0|0|0)
- 1:   Stiff tongue [HP:0031373](0|0) (0|0|0)
- 1:   Strawberry tongue [HP:0031042](0|0) (0|0|0)
- 1:   Tongue atrophy [HP:0012473](0|0) (0|0|0)
- 1:   Tongue nodules [HP:0000199](0|0) (0|0|0)
- 1:   Tongue telangiectasia [HP:0000227](0|0) (0|0|0)


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Family

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SCOP termFDR (all)Annotation (direct or inherited)
Laminin-type module0.002549Inherited
PDZ domain0.0498Inherited


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

Supra-domain (including individual superfamily)

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Supra-domain (Duplex) in N- to C-terminal order FDR (all) Annotation (direct or inherited)
57196,57196
  • 57196 - EGF/Laminin
  • 57196 - EGF/Laminin
  • 0.1569Inherited

    (show details)
    Supra-domain (Triple) in N- to C-terminal order FDR (all) Annotation (direct or inherited)
    57196,57196,57196
  • 57196 - EGF/Laminin
  • 57196 - EGF/Laminin
  • 57196 - EGF/Laminin
  • 0.0177Inherited