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Phenotypic Abnormality (PA): Generalized joint laxity

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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:   Phenotypic abnormality [HP:0000118] <25>
+ + + + 4:   Abnormality of the skeletal system [HP:0000924] <7>(88|98) (93|55|34)
+ + + 3:   Abnormality of skeletal physiology [HP:0011843] <8>(17|23) (17|15|15)
+ + 2:   Abnormality of joint mobility [HP:0011729] <6>(16|21) (16|15|15)
+ 1:   Joint laxity [HP:0001388] <2>(1|2) (1|1|0)
0:   Generalized joint laxity [HP:0002761](0|1) (0|0|0)


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

Family

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SCOP termFDR (all)Annotation (direct or inherited)
Rhodopsin-like0.000837Direct


Plot distribution on phylogenetic tree for Superfamily and/or Family domains annotated by this phenotype term
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