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Mammalian Phenotype (MP): abnormal spermiation

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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)
+ + + + + + 6:   mammalian phenotype [MP:0000001] <29>
+ + + + + 5:   reproductive system phenotype [MP:0005389] <2>(38|58) (47|18|6)
+ + + + 4:   abnormal reproductive system morphology [MP:0002160] <12>(28|46) (37|15|6)
+ + + 3:   abnormal gametogenesis [MP:0001929] <7>(15|19) (19|3|1)
+ + 2:   abnormal spermatogenesis [MP:0001156] <10>(8|13) (11|3|0)
+ 1:   abnormal spermiogenesis [MP:0001932] <3>(2|4) (4|1|0)
0:   abnormal spermiation [MP:0004182](0|1) (0|0|0)


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

Family

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SCOP termFDR (all)Annotation (direct or inherited)
PHD domain0.0001497Direct


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