SUPERFAMILY 1.75 HMM library and genome assignments server

SUPERFAMILY 2 can be accessed from supfam.org. Please contact us if you experience any problems.

Phenotypic Abnormality (PA): Foot osteomyelitis

(show info)

Jump to [ Top · Phenotype Hierarchy · Superfamily · Family · Supra-domain ]

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 immune system [HP:0002715] <3>(38|52) (40|29|16)
+ + + + 4:   Phenotypic abnormality [HP:0000118] <25>
+ + + + 4:   Abnormality of immune system physiology [HP:0010978] <14>(29|37) (31|22|11)
+ + + 3:   Abnormal inflammatory response [HP:0012647] <2>(17|20) (18|11|3)
+ + + 3:   Abnormality of the skeletal system [HP:0000924] <7>(88|98) (93|55|34)
+ + + 3:   Abnormality of limbs [HP:0040064] <8>(58|66) (63|33|25)
+ + 2:   Abnormality of skeletal physiology [HP:0011843] <8>(17|23) (17|15|15)
+ + 2:   Abnormality of the lower limb [HP:0002814] <17>(31|34) (35|15|13)
+ + 2:   Increased inflammatory response [HP:0012649] <27>(15|18) (16|9|3)
+ 1:   Abnormality of the foot [HP:0001760] <30>(20|24) (21|13|10)
+ 1:   Osteomyelitis [HP:0002754] <4>(0|0) (0|0|0)
0:   Foot osteomyelitis [HP:0001886](0|0) (0|0|0)