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Phenotypic Abnormality (PA): Insulin-resistant 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> #Domains
(Superfamily|Family)
#Supra-domain
(Single|Duplex|Triple)
+ + + + 4:   Abnormality of metabolism/homeostasis [HP:0001939] <16>(75|82) (79|40|16)
+ + + 3:   Phenotypic abnormality [HP:0000118] <25>
+ + + 3:   Abnormal homeostasis [HP:0012337] <8>(44|47) (44|22|8)
+ + 2:   Abnormality of the endocrine system [HP:0000818] <16>(28|35) (35|13|5)
+ + 2:   Abnormal glucose homeostasis [HP:0011014] <7>(11|12) (12|7|4)
+ + 2:   Glucose intolerance [HP:0001952] <2>(4|4) (5|3|3)
+ 1:   Diabetes mellitus [HP:0000819] <6>(3|3) (4|2|3)
+ 1:   Insulin resistance [HP:0000855] <1>(0|1) (0|0|0)
0:   Insulin-resistant diabetes mellitus [HP:0000831] <2>(0|0) (0|0|0)
- 1:   Neonatal insulin-dependent diabetes mellitus [HP:0000857] <1>(0|0) (0|0|0)
- 1:   Insulin-resistant diabetes mellitus at puberty [HP:0000877](0|0) (0|0|0)