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Mammalian Phenotype (MP): Leydig cell hypertrophy

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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:   endocrine/exocrine gland phenotype [MP:0005379] <2>(51|81) (55|36|12)
+ + + + + + + 7:   reproductive system phenotype [MP:0005389] <2>(38|58) (47|18|6)
+ + + + + + 6:   abnormal gland morphology [MP:0002163] <8>(44|71) (50|31|11)
+ + + + + + 6:   abnormal male reproductive system morphology [MP:0001145] <2>(12|18) (15|4|0)
+ + + + + + 6:   abnormal reproductive system morphology [MP:0002160] <12>(28|46) (37|15|6)
+ + + + + 5:   abnormal male genitalia morphology [MP:0009198] <2>(12|18) (15|4|0)
+ + + + + 5:   abnormal sex gland morphology [MP:0000653] <5>(20|29) (23|10|2)
+ + + + 4:   abnormal internal male genitalia morphology [MP:0009205] <10>(12|17) (15|4|0)
+ + + + 4:   abnormal male reproductive gland morphology [MP:0013325] <4>(10|15) (12|4|0)
+ + + 3:   abnormal testis morphology [MP:0001146] <15>(9|15) (11|4|0)
+ + 2:   abnormal seminiferous tubule morphology [MP:0002216] <6>(2|5) (3|1|0)
+ 1:   abnormal Leydig cell morphology [MP:0002786] <7>(0|1) (0|0|0)
0:   Leydig cell hypertrophy [MP:0013598](0|1) (0|0|0)


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Family

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SCOP termFDR (all)Annotation (direct or inherited)
Nuclear receptor0.0004881Direct


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