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Phenotypic Abnormality (PA): Type II diabetes mellitus

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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)
+ + + + + 5:   Abnormality of metabolism/homeostasis [HP:0001939] <16>(76|83) (79|38|16)
+ + + + 4:   Abnormal homeostasis [HP:0012337] <8>(42|43) (42|21|8)
+ + + 3:   Phenotypic abnormality [HP:0000118] <25>
+ + + 3:   Abnormal glucose homeostasis [HP:0011014] <7>(10|11) (11|7|4)
+ + 2:   Abnormality of the endocrine system [HP:0000818] <16>(30|34) (35|12|5)
+ + 2:   Glucose intolerance [HP:0001952] <2>(3|3) (4|3|3)
+ 1:   Diabetes mellitus [HP:0000819] <6>(2|2) (3|2|3)
0:   Type II diabetes mellitus [HP:0005978] <1>(0|0) (0|0|2)
- 1:   Insulin-dependent but ketosis-resistant diabetes [HP:0008205](0|0) (0|0|0)


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Supra-domain (including individual superfamily)

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Supra-domain (Triple) in N- to C-terminal order FDR (all) Annotation (direct or inherited)
57196,57184,57196
  • 57196 - EGF/Laminin
  • 57184 - Growth factor receptor domain
  • 57196 - EGF/Laminin
  • 0.0005496Direct
    57184,57196,57196
  • 57184 - Growth factor receptor domain
  • 57196 - EGF/Laminin
  • 57196 - EGF/Laminin
  • 0.0009817Direct