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Phenotypic Abnormality (PA): Short long bone

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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>(88|98) (93|54|34)
+ + + 3:   Abnormality of skeletal morphology [HP:0011842] <17>(86|89) (90|52|33)
+ + 2:   Abnormal appendicular skeleton morphology [HP:0011844] <4>(35|42) (39|23|23)
+ 1:   Abnormality of long bone morphology [HP:0011314] <18>(6|10) (6|3|1)
0:   Short long bone [HP:0003026] <7>(0|1) (0|1|1)
- 1:   Short metatarsal [HP:0010743] <5>(0|0) (0|0|0)
- 1:   Forearm undergrowth [HP:0009821] <3>(0|1) (0|0|0)
- 1:   Short tibia [HP:0005736] <3>(0|0) (0|0|0)
- 1:   Fibular hypoplasia [HP:0003038] <2>(0|0) (0|0|0)
- 1:   Short femur [HP:0003097](0|0) (0|0|0)
- 1:   Short humerus [HP:0005792](0|0) (0|0|0)
- 1:   Short tubular bones of the hand [HP:0001248](0|0) (0|0|0)


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Family

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SCOP termFDR (all)Annotation (direct or inherited)
RecA protein-like (ATPase-domain)0.03603Inherited


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Jump to [ Top · Phenotype Hierarchy · Superfamily · Family · Supra-domain ]

Supra-domain (including individual superfamily)

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Supra-domain (Duplex) in N- to C-terminal order FDR (all) Annotation (direct or inherited)
81296,81296
  • 81296 - E set domains
  • 81296 - E set domains
  • 0.0003383Direct

    (show details)
    Supra-domain (Triple) in N- to C-terminal order FDR (all) Annotation (direct or inherited)
    81296,81296,81296
  • 81296 - E set domains
  • 81296 - E set domains
  • 81296 - E set domains
  • 0.0003383Direct