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Mammalian Phenotype (MP): abnormal urine corticosterone 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)
+ + + + + + 6:   mammalian phenotype [MP:0000001] <29>
+ + + + + 5:   renal/urinary system phenotype [MP:0005367] <2>(41|47) (46|26|11)
+ + + + 4:   abnormal renal/urinary system physiology [MP:0005502] <6>(20|21) (25|10|1)
+ + + + 4:   homeostasis/metabolism phenotype [MP:0005376] <7>(140|174) (149|96|44)
+ + + 3:   abnormal homeostasis [MP:0001764] <27>(103|129) (113|73|31)
+ + + 3:   abnormal urine homeostasis [MP:0009643] <38>(9|7) (13|3|0)
+ + + 3:   abnormal lipid homeostasis [MP:0002118] <9>(25|29) (29|17|10)
+ + 2:   abnormal urine protein level [MP:0006315] <4>(0|1) (1|2|0)
+ + 2:   abnormal lipid level [MP:0001547] <16>(24|28) (26|16|10)
+ + 2:   abnormal hormone level [MP:0003953] <15>(27|29) (30|17|8)
+ 1:   abnormal urine hormone level [MP:0011538] <4>(0|0) (0|0|0)
+ 1:   abnormal corticosterone level [MP:0003963] <2>(1|1) (1|0|0)
0:   abnormal urine corticosterone level [MP:0011548] <2>(0|0) (0|0|0)
- 1:   decreased urine corticosterone level [MP:0011550](0|0) (0|0|0)
- 1:   increased urine corticosterone level [MP:0011549](0|0) (0|0|0)