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Phenotypic Abnormality (PA): Osteolysis

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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)
+ + 2:   Abnormality of skeletal morphology [HP:0011842] <17>(86|89) (90|52|33)
+ 1:   Abnormal bone structure [HP:0003330] <12>(4|3) (5|2|4)
0:   Osteolysis [HP:0002797] <4>(0|0) (0|0|0)
- 1:   Osteolysis involving bones of the upper limbs [HP:0045039] <4>(0|0) (0|0|0)
- 1:   Osteolysis involving bones of the lower limbs [HP:0009139] <2>(0|0) (0|0|0)
- 1:   Patchy reduction of bone mineral density [HP:0010657](0|0) (0|0|0)
- 1:   Progressive clavicular acroosteolysis [HP:0000905](0|0) (0|0|0)