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Mammalian Phenotype (MP): abnormal liver 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:   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:   abnormal ion homeostasis [MP:0001765] <15>(9|12) (11|4|0)
+ + + 3:   liver/biliary system phenotype [MP:0005370] <2>(37|39) (41|19|10)
+ + 2:   abnormal hepatobiliary system morphology [MP:0002138] <6>(25|32) (28|15|5)
+ + 2:   abnormal iron homeostasis [MP:0005637] <1>(0|0) (0|0|0)
+ + 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 liver morphology [MP:0000598] <26>(23|28) (26|13|5)
0:   abnormal liver iron level [MP:0008738] <2>(0|0) (0|0|0)
- 1:   decreased liver iron level [MP:0008743](0|0) (0|0|0)
- 1:   increased liver iron level [MP:0008807](0|0) (0|0|0)