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Mammalian Phenotype (MP): abnormal vitamin D 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:   homeostasis/metabolism phenotype [MP:0005376] <7>(140|174) (149|96|44)
+ + + + 4:   abnormal homeostasis [MP:0001764] <27>(103|129) (113|73|31)
+ + + 3:   abnormal vitamin homeostasis [MP:0004019] <3>(3|3) (3|0|0)
+ + + 3:   abnormal lipid homeostasis [MP:0002118] <9>(25|29) (29|17|10)
+ + 2:   abnormal lipid level [MP:0001547] <16>(24|28) (26|16|10)
+ + 2:   abnormal vitamin level [MP:0005400] <5>(3|3) (3|0|0)
+ 1:   abnormal sterol level [MP:0012224] <5>(11|13) (14|10|8)
+ 1:   abnormal fat-soluble vitamin level [MP:0005401] <3>(3|3) (3|0|0)
0:   abnormal vitamin D level [MP:0011228] <2>(0|0) (0|0|0)
- 1:   decreased vitamin D level [MP:0012336](0|0) (0|0|0)
- 1:   increased vitamin D level [MP:0012337](0|0) (0|0|0)