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Mammalian Phenotype (MP): abnormal cholangiocyte primary cilium morphology

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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> #Domains
(Superfamily|Family)
#Supra-domain
(Single|Duplex|Triple)
+ + + + + + 6:   mammalian phenotype [MP:0000001] <29>
+ + + + + 5:   cellular phenotype [MP:0005384] <6>(95|116) (103|56|31)
+ + + + + 5:   liver/biliary system phenotype [MP:0005370] <2>(37|39) (41|19|10)
+ + + + 4:   endocrine/exocrine gland phenotype [MP:0005379] <2>(51|81) (55|36|12)
+ + + + 4:   abnormal cell morphology [MP:0000358] <12>(19|19) (22|9|2)
+ + + + 4:   abnormal hepatobiliary system morphology [MP:0002138] <6>(25|32) (28|15|5)
+ + + 3:   abnormal gland morphology [MP:0002163] <8>(44|71) (50|31|11)
+ + + 3:   abnormal cilium morphology [MP:0013202] <2>(3|2) (3|3|1)
+ + + 3:   abnormal biliary tract morphology [MP:0005083] <4>(1|1) (1|0|0)
+ + 2:   abnormal primary cilium morphology [MP:0013203] <2>(3|2) (3|3|1)
+ + 2:   abnormal bile duct morphology [MP:0002928] <10>(1|1) (1|0|0)
+ 1:   abnormal cholangiocyte morphology [MP:0012236] <1>(0|0) (0|0|0)
+ 1:   abnormal nonmotile primary cilium morphology [MP:0013205] <7>(2|2) (2|2|1)
0:   abnormal cholangiocyte primary cilium morphology [MP:0012238](0|0) (0|0|0)