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Phenotypic Abnormality (PA): Sandal gap

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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>(89|98) (94|51|33)
+ + + + + 5:   Abnormality of skeletal morphology [HP:0011842] <18>(87|89) (90|49|32)
+ + + + + 5:   Phenotypic abnormality [HP:0000118] <25>
+ + + + 4:   Abnormality of limbs [HP:0040064] <8>(57|64) (59|32|25)
+ + + + 4:   Abnormal appendicular skeleton morphology [HP:0011844] <4>(35|41) (38|23|23)
+ + + + 4:   Abnormality of limb bone [HP:0040068] <1>(28|30) (30|18|20)
+ + + 3:   Abnormality of the lower limb [HP:0002814] <17>(30|31) (33|14|13)
+ + + 3:   Abnormality of limb bone morphology [HP:0002813] <13>(28|30) (30|18|20)
+ + 2:   Abnormality of the foot [HP:0001760] <30>(19|21) (19|12|10)
+ + 2:   Abnormal digit morphology [HP:0011297] <10>(16|19) (17|14|16)
+ 1:   Abnormality of toe [HP:0001780] <27>(7|6) (7|4|2)
0:   Sandal gap [HP:0001852](1|0) (0|0|0)


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

Superfamily

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SCOP termFDR (all)Annotation (direct or inherited)
SCOP hierarchy in SUPERFAMILY0.0009395Direct


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