SUPERFAMILY 1.75 HMM library and genome assignments server

Superfamily is undergoing a server migration - you are now browsing on the new server. Please contact us if you experience any problems.

Mammalian Phenotype (MP): abnormal sphingolipid level

(show info)

Jump to [ Top · Phenotype Hierarchy · Superfamily · Family · Supra-domain ]

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:   mammalian phenotype [MP:0000001] <29>
+ + + + 4:   homeostasis/metabolism phenotype [MP:0005376] <7>(140|174) (149|96|44)
+ + + 3:   abnormal homeostasis [MP:0001764] <27>(103|129) (113|73|31)
+ + 2:   abnormal lipid homeostasis [MP:0002118] <9>(25|29) (29|17|10)
+ 1:   abnormal lipid level [MP:0001547] <16>(24|28) (26|16|10)
0:   abnormal sphingolipid level [MP:0012230] <4>(0|0) (0|0|0)
- 1:   abnormal sphingosine level [MP:0020115] <2>(0|0) (0|0|0)
- 1:   abnormal ceramide level [MP:0012232] <1>(0|0) (0|0|0)
- 1:   abnormal glycosphingolipid level [MP:0020194] <1>(0|0) (0|0|0)
- 1:   abnormal sphingomyelin level [MP:0009823] <1>(0|0) (0|0|0)