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Phenotypic Abnormality (PA): Neck muscle weakness

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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)
+ + + + 4:   Phenotypic abnormality [HP:0000118] <25>
+ + + 3:   Abnormality of the musculature [HP:0003011] <3>(64|83) (70|33|9)
+ + 2:   Abnormal muscle physiology [HP:0011804] <12>(44|59) (51|22|5)
+ 1:   Muscle weakness [HP:0001324] <22>(13|14) (15|4|0)
0:   Neck muscle weakness [HP:0000467] <1>(3|3) (3|1|0)
- 1:   Neck flexor weakness [HP:0003722](2|2) (2|1|0)


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Superfamily

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SCOP termFDR (all)Annotation (direct or inherited)
Tropomyosin0.0008638Direct
Neurotransmitter-gated ion-channel transmembrane pore0.001188Inherited
Nicotinic receptor ligand binding domain-like0.001188Inherited


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Family

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SCOP termFDR (all)Annotation (direct or inherited)
Tropomyosin0.0005076Direct
Neurotransmitter-gated ion-channel transmembrane pore0.000719Direct
Nicotinic receptor ligand binding domain-like0.000719Direct


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)
Tropomyosin0.0004522Direct
Nicotinic receptor ligand binding domain-like0.0006358Direct
Neurotransmitter-gated ion-channel transmembrane pore0.0006358Direct

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Supra-domain (Duplex) in N- to C-terminal order FDR (all) Annotation (direct or inherited)
63712,90112
  • 63712 - Nicotinic receptor ligand binding domain-like
  • 90112 - Neurotransmitter-gated ion-channel transmembrane pore
  • 0.0006358Direct


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