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Phenotypic Abnormality (PA): Arachnodactyly

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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:   Abnormality of the skeletal system [HP:0000924] <7>(89|98) (94|51|33)
+ + + + + + 6:   Phenotypic abnormality [HP:0000118] <25>
+ + + + + + 6:   Abnormality of skeletal morphology [HP:0011842] <18>(87|89) (90|49|32)
+ + + + + 5:   Abnormal appendicular skeleton morphology [HP:0011844] <4>(35|41) (38|23|23)
+ + + + + 5:   Abnormality of limb bone [HP:0040068] <1>(28|30) (30|18|20)
+ + + + + 5:   Abnormality of limbs [HP:0040064] <8>(57|64) (59|32|25)
+ + + + 4:   Abnormality of limb bone morphology [HP:0002813] <13>(28|30) (30|18|20)
+ + + + 4:   Abnormality of the upper limb [HP:0002817] <20>(26|29) (30|18|16)
+ + + 3:   Abnormality of the hand [HP:0001155] <26>(20|25) (24|16|14)
+ + + 3:   Abnormal digit morphology [HP:0011297] <10>(16|19) (17|14|16)
+ + 2:   Abnormality of finger [HP:0001167] <24>(11|14) (12|10|10)
+ 1:   Slender finger [HP:0001238] <1>(0|1) (1|2|0)
+ 1:   Long fingers [HP:0100807] <2>(0|1) (0|1|0)
0:   Arachnodactyly [HP:0001166](0|0) (0|1|0)


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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)
57184,57184
  • 57184 - Growth factor receptor domain
  • 57184 - Growth factor receptor domain
  • 0.0008324Direct