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Phenotypic Abnormality (PA): Thickened cortex of long bones

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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 bone structure [HP:0003330] <12>(4|3) (5|2|4)
+ + 2:   Abnormal cortical bone morphology [HP:0003103] <8>(0|0) (0|0|0)
+ + 2:   Abnormal appendicular skeleton morphology [HP:0011844] <4>(35|43) (39|23|23)
+ 1:   Abnormality of long bone morphology [HP:0011314] <18>(6|10) (6|3|1)
+ 1:   Thickened cortex of bones [HP:0100039] <2>(0|0) (0|0|0)
0:   Thickened cortex of long bones [HP:0000935] <4>(0|0) (0|0|0)
- 1:   Cortical thickening of long bone diaphyses [HP:0005791](0|0) (0|0|0)
- 1:   Cortically dense long tubular bones [HP:0006415](0|0) (0|0|0)
- 1:   Humeral cortical thickening [HP:0003868](0|0) (0|0|0)
- 1:   Massively thickened long bone cortices [HP:0005665](0|0) (0|0|0)