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

Phenotypic Abnormality (PA): Absent ray

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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> #Domains
(Superfamily|Family)
#Supra-domain
(Single|Duplex|Triple)
+ + + + 4:   Phenotypic abnormality [HP:0000118] <25>
+ + + 3:   Abnormality of the skeletal system [HP:0000924] <7>(88|98) (93|55|34)
+ + + 3:   Abnormality of skeletal morphology [HP:0011842] <17>(86|89) (90|52|33)
+ + + 3:   Abnormality of limbs [HP:0040064] <8>(58|66) (63|33|25)
+ + 2:   Abnormality of limb bone [HP:0040068] <1>(29|32) (33|18|20)
+ + 2:   Abnormal appendicular skeleton morphology [HP:0011844] <4>(35|43) (39|23|23)
+ 1:   Abnormality of limb bone morphology [HP:0002813] <13>(29|32) (32|18|20)
0:   Absent ray [HP:0030030](0|0) (0|0|0)