SUPERFAMILY 1.75 HMM library and genome assignments server

Superfamily is undergoing a server migration - you are now browsing on the new server. Please contact us if you experience any problems.

Phenotypic Abnormality (PA): Upper limb phocomelia

(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 skeletal system [HP:0000924] <7>(88|98) (93|54|34)
+ + + + 4:   Abnormality of skeletal morphology [HP:0011842] <17>(86|89) (90|52|33)
+ + + + 4:   Abnormality of limb bone [HP:0040068] <1>(29|31) (33|18|20)
+ + + + 4:   Phenotypic abnormality [HP:0000118] <25>
+ + + 3:   Abnormality of limb bone morphology [HP:0002813] <13>(29|31) (32|18|20)
+ + + 3:   Aplasia/hypoplasia involving the skeleton [HP:0009115] <2>(13|11) (15|10|17)
+ + + 3:   Abnormal appendicular skeleton morphology [HP:0011844] <4>(35|42) (39|23|23)
+ + + 3:   Abnormality of limbs [HP:0040064] <8>(58|65) (63|33|25)
+ + 2:   Abnormality of long bone morphology [HP:0011314] <18>(6|10) (6|3|1)
+ + 2:   Aplasia/hypoplasia of the extremities [HP:0009815] <6>(8|9) (10|3|5)
+ + 2:   Aplasia/hypoplasia involving bones of the extremities [HP:0045060] <3>(7|8) (9|3|5)
+ + 2:   Abnormality of the upper limb [HP:0002817] <20>(29|34) (35|17|16)
+ 1:   Phocomelia [HP:0009829] <3>(0|0) (0|0|0)
+ 1:   Aplasia/hypoplasia involving bones of the upper limbs [HP:0006496] <8>(3|7) (6|2|4)
0:   Upper limb phocomelia [HP:0009813](0|0) (0|0|0)