SUPERFAMILY 1.75 HMM library and genome assignments server

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Phenotypic Abnormality (PA): Insulin resistance

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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)
+ + + + 4:   Phenotypic abnormality [HP:0000118] <25>
+ + + 3:   Abnormality of metabolism/homeostasis [HP:0001939] <16>(76|83) (79|38|16)
+ + 2:   Abnormal homeostasis [HP:0012337] <8>(42|43) (42|21|8)
+ 1:   Abnormal glucose homeostasis [HP:0011014] <7>(10|11) (11|7|4)
0:   Insulin resistance [HP:0000855] <1>(0|1) (0|0|0)
- 1:   Insulin-resistant diabetes mellitus [HP:0000831] <2>(0|0) (0|0|0)


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

Family

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SCOP termFDR (all)Annotation (direct or inherited)
Phosphotyrosine-binding domain (PTB)0.0001791Direct


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