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Phenotypic Abnormality (PA): Weakness of facial musculature

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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)
+ + + + + 5:   Abnormality of head or neck [HP:0000152] <2>(86|104) (97|58|38)
+ + + + 4:   Phenotypic abnormality [HP:0000118] <25>
+ + + + 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)
+ + + 3:   Abnormality of the musculature [HP:0003011] <3>(64|83) (70|33|9)
+ + 2:   Abnormality of facial soft tissue [HP:0011799] <7>(2|3) (4|3|0)
+ + 2:   Abnormal skeletal muscle morphology [HP:0011805] <38>(30|36) (35|14|4)
+ 1:   Abnormality of facial musculature [HP:0000301] <12>(2|3) (4|3|0)
0:   Weakness of facial musculature [HP:0030319] <3>(0|1) (1|1|0)
- 1:   Facial palsy [HP:0010628] <4>(0|0) (0|1|0)
- 1:   Facial paralysis [HP:0007209](0|0) (0|0|0)
- 1:   Weakness of orbicularis oculi muscle [HP:0012507](0|0) (0|0|0)


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Family

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SCOP termFDR (all)Annotation (direct or inherited)
Kelch motif0.0007307Direct


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)
Kelch motif0.0005589Direct

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Supra-domain (Duplex) in N- to C-terminal order FDR (all) Annotation (direct or inherited)
53300,53300
  • 53300 - vWA-like
  • 53300 - vWA-like
  • 0.0003347Direct


    Plot distribution on phylogenetic tree for Supra-domains (Single/Individual) annotated by this phenotype term
    Plot tree as:   Download Newick format tree:
    (show help)