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Phenotypic Abnormality (PA): Flexion contracture of digit

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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:   Abnormality of the skeletal system [HP:0000924] <7>(88|98) (93|54|34)
+ + + 3:   Abnormality of skeletal physiology [HP:0011843] <8>(17|23) (17|15|15)
+ + + 3:   Phenotypic abnormality [HP:0000118] <25>
+ + + 3:   Abnormality of skeletal morphology [HP:0011842] <17>(86|89) (90|52|33)
+ + + 3:   Abnormality of the musculature [HP:0003011] <3>(64|83) (70|33|9)
+ + 2:   Abnormal tendon morphology [HP:0100261] <8>(8|10) (8|7|1)
+ + 2:   Abnormality of connective tissue [HP:0003549] <12>(19|27) (19|20|20)
+ + 2:   Abnormal skeletal muscle morphology [HP:0011805] <38>(30|36) (35|14|4)
+ + 2:   Abnormality of joint mobility [HP:0011729] <6>(16|21) (16|15|15)
+ 1:   Flexion contracture [HP:0001371] <9>(8|10) (8|7|1)
0:   Flexion contracture of digit [HP:0030044] <3>(0|1) (0|3|0)
- 1:   Flexion contracture of finger [HP:0012785] <6>(0|1) (0|3|0)
- 1:   Flexion contracture of toe [HP:0005830] <6>(0|0) (0|0|0)
- 1:   Camptodactyly [HP:0012385] <2>(0|1) (0|2|0)


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Family

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SCOP termFDR (all)Annotation (direct or inherited)
Integrin A (or I) domain0.06391Inherited


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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
  • 0.0006894Direct
    50729,50729
  • 50729 - PH domain-like
  • 50729 - PH domain-like
  • 0.003295Inherited
    57196,57196
  • 57196 - EGF/Laminin
  • 57196 - EGF/Laminin
  • 0.0108Inherited