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Mammalian Phenotype (MP): abnormal Harderian gland pigmentation

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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)
+ + + + + 5:   endocrine/exocrine gland phenotype [MP:0005379] <2>(51|81) (55|36|12)
+ + + + 4:   abnormal gland morphology [MP:0002163] <8>(44|71) (50|31|11)
+ + + 3:   mammalian phenotype [MP:0000001] <29>
+ + + 3:   abnormal exocrine gland morphology [MP:0013558] <13>(18|22) (19|13|8)
+ + 2:   abnormal merocrine gland morphology [MP:0013544] <3>(2|2) (2|1|0)
+ + 2:   pigmentation phenotype [MP:0001186] <13>(4|5) (6|1|3)
+ 1:   abnormal extracutaneous pigmentation [MP:0009389] <4>(1|1) (2|0|1)
+ 1:   abnormal Harderian gland morphology [MP:0005248] <4>(2|2) (2|1|0)
0:   abnormal Harderian gland pigmentation [MP:0003798](0|0) (0|0|0)