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Phenotypic Abnormality (PA): Shoulder dislocation

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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)
+ + + + + 5:   Phenotypic abnormality [HP:0000118] <25>
+ + + + 4:   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:   Abnormal axial skeleton morphology [HP:0009121] <6>(47|61) (51|30|26)
+ + + 3:   Abnormal joint morphology [HP:0001367] <18>(19|23) (20|9|2)
+ + 2:   Joint dislocation [HP:0001373] <6>(6|9) (7|2|0)
+ + 2:   Abnormal appendicular skeleton morphology [HP:0011844] <4>(35|43) (39|23|23)
+ + 2:   Abnormality of the thorax [HP:0000765] <12>(13|18) (14|8|7)
+ 1:   Abnormality of the shoulder [HP:0003043] <11>(0|0) (0|0|0)
+ 1:   Upper extremity joint dislocation [HP:0030310] <3>(1|2) (1|0|0)
0:   Shoulder dislocation [HP:0003834] <1>(0|0) (0|0|0)
- 1:   Recurrent shoulder dislocation [HP:0031610](0|0) (0|0|0)