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Mammalian Phenotype (MP): abnormal intestinal 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> (#SF|#FA) #Supra-domain
(Single|Duplex|Triple)
+ + + + + 5:   homeostasis/metabolism phenotype [MP:0005376] <7>(140|174) (149|96|44)
+ + + + 4:   abnormal homeostasis [MP:0001764] <27>(103|129) (113|73|31)
+ + + + 4:   mammalian phenotype [MP:0000001] <29>
+ + + 3:   abnormal mineral homeostasis [MP:0005636] <4>(5|6) (5|1|0)
+ + + 3:   digestive/alimentary phenotype [MP:0005381] <2>(38|46) (40|19|9)
+ + + 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 digestive system morphology [MP:0000462] <21>(30|38) (31|13|3)
+ + 2:   abnormal mineral level [MP:0000192] <4>(3|4) (3|1|0)
+ 1:   abnormal iron level [MP:0001770] <10>(0|0) (0|0|0)
+ 1:   abnormal intestine morphology [MP:0000477] <17>(10|14) (11|9|2)
0:   abnormal intestinal iron level [MP:0008740] <2>(0|0) (0|0|0)
- 1:   decreased intestinal iron level [MP:0020385](0|0) (0|0|0)
- 1:   increased intestinal iron level [MP:0020369](0|0) (0|0|0)