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Phenotypic Abnormality (PA): Anomaly of the upper limb diaphyses

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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)
+ + + + 4:   Abnormality of the skeletal system [HP:0000924] <7>(88|98) (93|55|34)
+ + + + 4:   Abnormality of skeletal morphology [HP:0011842] <17>(86|89) (90|52|33)
+ + + 3:   Abnormality of long bone morphology [HP:0011314] <18>(6|10) (6|3|1)
+ + + 3:   Abnormal appendicular skeleton morphology [HP:0011844] <4>(35|43) (39|23|23)
+ + + 3:   Abnormality of limb bone [HP:0040068] <1>(29|32) (33|18|20)
+ + + 3:   Phenotypic abnormality [HP:0000118] <25>
+ + 2:   Abnormal diaphysis morphology [HP:0000940] <9>(0|1) (0|0|0)
+ + 2:   Abnormality of limbs [HP:0040064] <8>(58|66) (63|33|25)
+ + 2:   Abnormality of limb bone morphology [HP:0002813] <13>(29|32) (32|18|20)
+ 1:   Anomaly of the limb diaphyses [HP:0006504] <6>(0|1) (0|0|0)
+ 1:   Abnormality of the upper limb [HP:0002817] <20>(29|35) (35|17|16)
0:   Anomaly of the upper limb diaphyses [HP:0009808] <7>(0|0) (0|0|0)
- 1:   Abnormality of the humeral diaphysis [HP:0003926] <10>(0|0) (0|0|0)
- 1:   Abnormality of radial diaphysis [HP:0004027] <4>(0|0) (0|0|0)
- 1:   Broad diaphyses of the upper limbs [HP:0003861] <1>(0|0) (0|0|0)
- 1:   Cortical diaphyseal irregularity of the upper limbs [HP:0003858] <1>(0|0) (0|0|0)
- 1:   Cortical diaphyseal thickening of the upper limbs [HP:0003859] <1>(0|0) (0|0|0)
- 1:   Diaphyseal sclerosis of the upper limbs [HP:0003860] <1>(0|0) (0|0|0)
- 1:   Abnormalities of the diaphyses of the hand [HP:0005925](0|0) (0|0|0)