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Phenotypic Abnormality (PA): Craniofacial dystonia

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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 nervous system [HP:0000707] <4>(142|168) (156|103|45)
+ + + + 4:   Abnormality of nervous system physiology [HP:0012638] <26>(101|119) (112|81|39)
+ + + 3:   Abnormality of movement [HP:0100022] <19>(23|25) (25|14|3)
+ + 2:   Dystonia [HP:0001332] <8>(1|2) (1|1|0)
+ 1:   Focal dystonia [HP:0004373] <3>(1|2) (1|1|0)
0:   Craniofacial dystonia [HP:0012179] <5>(1|1) (1|1|0)
- 1:   Torticollis [HP:0000473] <1>(1|1) (1|1|0)
- 1:   Blepharospasm [HP:0000643](0|0) (0|0|0)
- 1:   Lingual dystonia [HP:0031008](0|0) (0|0|0)
- 1:   Orofacial action-specific dystonia induced by speech [HP:0031007](0|0) (0|0|0)
- 1:   Oromandibular dystonia [HP:0012048](0|0) (0|0|0)


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Superfamily

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SCOP termFDR (all)Annotation (direct or inherited)
vWA-like0.002404Inherited


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Family

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SCOP termFDR (all)Annotation (direct or inherited)
Integrin A (or I) domain0.0001481Direct


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)
vWA-like0.001371Inherited

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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
  • 0.000007191Direct


    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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