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Phenotypic Abnormality (PA): Abnormality of the cervical spine

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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:   Phenotypic abnormality [HP:0000118] <25>
+ + + + 4:   Abnormality of the skeletal system [HP:0000924] <7>(89|98) (94|51|33)
+ + + 3:   Abnormality of skeletal morphology [HP:0011842] <18>(87|89) (90|49|32)
+ + 2:   Abnormal axial skeleton morphology [HP:0009121] <6>(48|61) (53|28|26)
+ 1:   Abnormality of the vertebral column [HP:0000925] <20>(21|27) (25|11|10)
0:   Abnormality of the cervical spine [HP:0003319] <14>(3|5) (4|2|1)
- 1:   Aplasia/Hypoplasia of the cervical spine [HP:0011041] <3>(0|0) (0|0|0)
- 1:   Cervical subluxation [HP:0003308] <2>(0|0) (0|0|0)
- 1:   Abnormal cervical curvature [HP:0005905] <1>(2|2) (2|1|0)
- 1:   C1-C2 vertebral abnormality [HP:0008440] <1>(0|0) (0|0|0)
- 1:   Cervical platyspondyly [HP:0004558](0|0) (0|0|0)
- 1:   Cervical spine hypermobility [HP:0003318](0|0) (0|0|0)
- 1:   Cervical spine instability [HP:0010646](0|0) (0|0|0)
- 1:   Cervical spondylosis [HP:0008480](0|0) (0|0|0)
- 1:   Cervical vertebral bodies with decreased anteroposterior diameter [HP:0008483](0|0) (0|0|0)
- 1:   Cervical vertebral dysplasia [HP:0008469](0|0) (0|0|0)
- 1:   Decreased cervical spine mobility [HP:0004637](1|1) (1|0|0)
- 1:   Enlarged sagittal diameter of the cervical canal [HP:0005878](0|0) (0|0|0)
- 1:   Short neck [HP:0000470](0|2) (1|1|1)
- 1:   Widening of cervical spinal canal [HP:0004571](0|0) (0|0|0)


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Superfamily

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SCOP termFDR (all)Annotation (direct or inherited)
Nicotinic receptor ligand binding domain-like0.1374Inherited
Neurotransmitter-gated ion-channel transmembrane pore0.1374Inherited
Homeodomain-like0.216Inherited


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Family

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SCOP termFDR (all)Annotation (direct or inherited)
Actin/HSP700.008168Inherited
T-box0.02559Inherited
Nicotinic receptor ligand binding domain-like0.115Inherited
Neurotransmitter-gated ion-channel transmembrane pore0.115Inherited
Homeodomain0.1638Inherited


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)
GroEL equatorial domain-like0.02196Inherited
Nicotinic receptor ligand binding domain-like0.112Inherited
Neurotransmitter-gated ion-channel transmembrane pore0.112Inherited
Homeodomain-like0.1826Inherited

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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
  • 0.001046Inherited
    63712,90112
  • 63712 - Nicotinic receptor ligand binding domain-like
  • 90112 - Neurotransmitter-gated ion-channel transmembrane pore
  • 0.112Inherited

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    Supra-domain (Triple) in N- to C-terminal order FDR (all) Annotation (direct or inherited)
    57184,57196,57184
  • 57184 - Growth factor receptor domain
  • 57196 - EGF/Laminin
  • 57184 - Growth factor receptor domain
  • 0.02196Inherited


    Plot distribution on phylogenetic tree for Supra-domains (Single/Individual) annotated by this phenotype term
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