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Phenotypic Abnormality (PA): Cross-fusion of the forearm 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> (#SF|#FA) #Supra-domain
(Single|Duplex|Triple)
+ + + + + 5:   Phenotypic abnormality [HP:0000118] <25>
+ + + + + 5:   Abnormality of the skeletal system [HP:0000924] <7>(88|98) (93|54|34)
+ + + + + 5:   Abnormality of skeletal morphology [HP:0011842] <17>(86|89) (90|52|33)
+ + + + 4:   Abnormal appendicular skeleton morphology [HP:0011844] <4>(35|42) (39|23|23)
+ + + + 4:   Abnormality of limb bone [HP:0040068] <1>(29|31) (33|18|20)
+ + + + 4:   Abnormality of limbs [HP:0040064] <8>(58|65) (63|33|25)
+ + + 3:   Abnormality of limb bone morphology [HP:0002813] <13>(29|31) (32|18|20)
+ + + 3:   Abnormality of the upper limb [HP:0002817] <20>(29|34) (35|17|16)
+ + 2:   Abnormality of the forearm [HP:0002973] <7>(4|4) (5|2|1)
+ + 2:   Abnormal upper limb bone morphology [HP:0040070] <5>(5|4) (6|2|1)
+ 1:   Abnormality of forearm bone [HP:0040072] <13>(4|4) (5|2|1)
0:   Cross-fusion of the forearm bones [HP:0003958](0|0) (0|0|0)