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Phenotypic Abnormality (PA): Abnormal foot bone ossification

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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:   Abnormality of the skeletal system [HP:0000924] <7>(88|98) (93|55|34)
+ + + + 4:   Phenotypic abnormality [HP:0000118] <25>
+ + + + 4:   Abnormality of skeletal morphology [HP:0011842] <17>(86|89) (90|52|33)
+ + + 3:   Abnormality of limbs [HP:0040064] <8>(58|66) (63|33|25)
+ + + 3:   Abnormal bone structure [HP:0003330] <12>(4|3) (5|2|4)
+ + 2:   Abnormality of the lower limb [HP:0002814] <17>(31|34) (35|15|13)
+ + 2:   Abnormal bone ossification [HP:0011849] <5>(4|2) (4|0|2)
+ 1:   Abnormality of the foot [HP:0001760] <30>(20|24) (21|13|10)
+ 1:   Abnormal enchondral ossification [HP:0003336] <12>(2|0) (2|0|0)
0:   Abnormal foot bone ossification [HP:0010675] <2>(0|0) (0|0|0)
- 1:   Abnormal tarsal ossification [HP:0008369] <5>(0|0) (0|0|0)
- 1:   Abnormal metatarsal ossification [HP:0008371] <1>(0|0) (0|0|0)