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Mammalian Phenotype (MP): abnormal kidney iron level

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Root: MP Hierarchy (mammalian/mouse phenotype from MGI_4.41)

Shortest distance to current term
(+ for parents, - for children)
MP term [MP ID] <#Children> #Domains
(Superfamily|Family)
#Supra-domain
(Single|Duplex|Triple)
+ + + + + 5:   homeostasis/metabolism phenotype [MP:0005376] <7>(140|174) (149|96|44)
+ + + + 4:   mammalian phenotype [MP:0000001] <29>
+ + + + 4:   abnormal homeostasis [MP:0001764] <27>(103|129) (113|73|31)
+ + + 3:   abnormal mineral homeostasis [MP:0005636] <4>(5|6) (5|1|0)
+ + + 3:   renal/urinary system phenotype [MP:0005367] <2>(41|47) (46|26|11)
+ + + 3:   abnormal ion homeostasis [MP:0001765] <15>(9|12) (11|4|0)
+ + 2:   abnormal iron homeostasis [MP:0005637] <1>(0|0) (0|0|0)
+ + 2:   abnormal mineral level [MP:0000192] <4>(3|4) (3|1|0)
+ + 2:   abnormal renal/urinary system morphology [MP:0000516] <14>(31|36) (36|22|11)
+ 1:   abnormal kidney morphology [MP:0002135] <29>(26|28) (28|15|6)
+ 1:   abnormal iron level [MP:0001770] <10>(0|0) (0|0|0)
0:   abnormal kidney iron level [MP:0008742] <2>(0|0) (0|0|0)
- 1:   decreased kidney iron level [MP:0010376](0|0) (0|0|0)
- 1:   increased kidney iron level [MP:0010375](0|0) (0|0|0)