dcGO - A comprehensive domain-centric ontology resource for post-genomic research on functions, phenotypes, diseases and more   
  
  

Phenotypic Abnormality (PA): Morbus Scheuermann

(show info)

Jump to [ Top · Hierarchy · Annotations ]

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> #Domains
(Superfamily|Family)
#Supra-domain
(Single|Duplex|Triple)
+ + + + + 5:   Phenotypic abnormality [HP:0000118] <25>
+ + + + 4:   Abnormality of skeletal morphology [HP:0011842] <17>(86|89) (90|52|33)
+ + + + 4:   Abnormality of the skeletal system [HP:0000924] <7>(88|98) (93|55|34)
+ + + 3:   Abnormality of skeletal physiology [HP:0011843] <8>(17|23) (17|15|15)
+ + + 3:   Abnormal axial skeleton morphology [HP:0009121] <6>(47|61) (51|30|26)
+ + 2:   Abnormality of the vertebral column [HP:0000925] <20>(22|27) (25|11|10)
+ + 2:   Avascular necrosis [HP:0010885] <1>(0|0) (0|0|0)
+ 1:   Abnormal vertebral morphology [HP:0003468] <16>(7|6) (8|1|2)
+ 1:   Juvenile aseptic necrosis [HP:0100323] <6>(0|0) (0|0|0)
0:   Morbus Scheuermann [HP:0010891] <1>(0|0) (0|0|0)
- 1:   Scheuermann-like vertebral changes [HP:0008478](0|0) (0|0|0)