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Mammalian Phenotype (MP): impaired ovarian folliculogenesis

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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)
+ + + + + + + + + 9:   mammalian phenotype [MP:0000001] <29>
+ + + + + + + 7:   reproductive system phenotype [MP:0005389] <2>(38|58) (47|18|6)
+ + + + + + + 7:   endocrine/exocrine gland phenotype [MP:0005379] <2>(51|81) (55|36|12)
+ + + + + + 6:   abnormal reproductive system morphology [MP:0002160] <12>(28|46) (37|15|6)
+ + + + + + 6:   abnormal female reproductive system morphology [MP:0001119] <2>(13|22) (17|8|2)
+ + + + + + 6:   abnormal gland morphology [MP:0002163] <8>(44|71) (50|31|11)
+ + + + + 5:   abnormal sex gland morphology [MP:0000653] <5>(20|29) (23|10|2)
+ + + + + 5:   abnormal female genitalia morphology [MP:0009208] <2>(13|22) (17|8|2)
+ + + + 4:   abnormal female reproductive gland morphology [MP:0013324] <6>(10|15) (11|6|2)
+ + + + 4:   abnormal internal female genitalia morphology [MP:0009209] <6>(12|21) (16|8|2)
+ + + 3:   abnormal ovary morphology [MP:0001126] <14>(9|14) (10|4|2)
+ + 2:   abnormal ovarian follicle morphology [MP:0001131] <9>(3|7) (4|0|0)
+ 1:   abnormal ovarian folliculogenesis [MP:0001130] <4>(2|4) (3|0|0)
0:   impaired ovarian folliculogenesis [MP:0001129](0|1) (0|0|0)


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Family

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SCOP termFDR (all)Annotation (direct or inherited)
Forkhead DNA-binding domain0.0005287Direct


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