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Phenotypic Abnormality (PA): Myopathy

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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)
+ + + 3:   Phenotypic abnormality [HP:0000118] <25>
+ + 2:   Abnormality of the musculature [HP:0003011] <3>(64|83) (70|33|9)
+ 1:   Abnormal skeletal muscle morphology [HP:0011805] <38>(30|36) (35|14|4)
0:   Myopathy [HP:0003198] <6>(0|1) (0|1|1)
- 1:   Minicore myopathy [HP:0003789] <1>(0|0) (0|0|0)
- 1:   EMG: myopathic abnormalities [HP:0003458](0|0) (0|1|0)
- 1:   Inflammatory myopathy [HP:0009071](0|0) (0|0|0)
- 1:   Myofibrillar myopathy [HP:0003715](0|0) (0|0|0)
- 1:   Necrotizing myopathy [HP:0008978](0|0) (0|0|0)
- 1:   Skeletal myopathy [HP:0003756](0|0) (0|0|0)


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Family

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SCOP termFDR (all)Annotation (direct or inherited)
LIM domain0.0005515Direct


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Supra-domain (including individual superfamily)

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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
  • 0.000797Direct

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    Supra-domain (Triple) in N- to C-terminal order FDR (all) Annotation (direct or inherited)
    57716,57716,57716
  • 57716 - Glucocorticoid receptor-like (DNA-binding domain)
  • 57716 - Glucocorticoid receptor-like (DNA-binding domain)
  • 57716 - Glucocorticoid receptor-like (DNA-binding domain)
  • 0.0004421Direct