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Mammalian Phenotype (MP): abnormal renal phosphate reabsorbtion

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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)
+ + + + 4:   mammalian phenotype [MP:0000001] <29>
+ + + + 4:   renal/urinary system phenotype [MP:0005367] <2>(41|47) (46|26|11)
+ + + 3:   homeostasis/metabolism phenotype [MP:0005376] <7>(140|174) (149|96|44)
+ + + 3:   abnormal renal/urinary system physiology [MP:0005502] <6>(20|21) (25|10|1)
+ + 2:   abnormal homeostasis [MP:0001764] <27>(103|129) (113|73|31)
+ + 2:   abnormal kidney physiology [MP:0002136] <22>(12|15) (14|5|1)
+ 1:   abnormal renal reabsorbtion [MP:0010107] <6>(2|2) (3|0|0)
+ 1:   abnormal ion homeostasis [MP:0001765] <15>(9|12) (11|4|0)
0:   abnormal renal phosphate reabsorbtion [MP:0010110](0|0) (0|0|0)