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Phenotypic Abnormality (PA): Abnormality of upper limb metaphysis

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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 skeletal morphology [HP:0011842] <17>(86|89) (90|52|33)
+ + + + 4:   Abnormality of the skeletal system [HP:0000924] <7>(88|98) (93|54|34)
+ + + 3:   Abnormality of limb bone [HP:0040068] <1>(29|31) (33|18|20)
+ + + 3:   Abnormal appendicular skeleton morphology [HP:0011844] <4>(35|42) (39|23|23)
+ + + 3:   Phenotypic abnormality [HP:0000118] <25>
+ + 2:   Abnormality of limb bone morphology [HP:0002813] <13>(29|31) (32|18|20)
+ + 2:   Abnormality of long bone morphology [HP:0011314] <18>(6|10) (6|3|1)
+ + 2:   Abnormality of limbs [HP:0040064] <8>(58|65) (63|33|25)
+ 1:   Abnormality of the metaphysis [HP:0000944] <19>(2|5) (2|1|0)
+ 1:   Abnormality of the upper limb [HP:0002817] <20>(29|34) (35|17|16)
0:   Abnormality of upper limb metaphysis [HP:0009809] <12>(0|0) (0|0|0)
- 1:   Abnormality of the humeral metaphyses [HP:0003907] <14>(0|0) (0|0|0)
- 1:   Abnormality of radial metaphyses [HP:0004015] <10>(0|0) (0|0|0)
- 1:   Abnormality of ulnar metaphysis [HP:0004039] <8>(0|0) (0|0|0)
- 1:   Abnormality of the elbow metaphyses [HP:0003949] <3>(0|0) (0|0|0)
- 1:   Sclerosis of metaphyses of the upper limbs [HP:0003854] <3>(0|0) (0|0|0)
- 1:   Upper limb metaphyseal widening [HP:0003856] <3>(0|0) (0|0|0)
- 1:   Upper-limb metaphyseal irregularity [HP:0003850] <3>(0|0) (0|0|0)
- 1:   Lytic defects in metaphyses of the upper limbs [HP:0003851] <2>(0|0) (0|0|0)
- 1:   Abnormalities of the metaphyses of the hand [HP:0005923] <1>(0|0) (0|0|0)
- 1:   Cupped metaphyses of the upper limbs [HP:0003848] <1>(0|0) (0|0|0)
- 1:   Normal density transverse bands in metaphyses of the upper limbs [HP:0003852] <1>(0|0) (0|0|0)
- 1:   Spurred metaphyses of the upper limbs [HP:0003855] <1>(0|0) (0|0|0)