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Mammalian Phenotype (MP): abnormal secondary sex determination

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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)
+ + + + 4:   mammalian phenotype [MP:0000001] <29>
+ + + 3:   reproductive system phenotype [MP:0005389] <2>(38|58) (47|18|6)
+ + 2:   abnormal reproductive system morphology [MP:0002160] <12>(28|46) (37|15|6)
+ 1:   abnormal sex determination [MP:0002210] <3>(7|18) (12|6|3)
0:   abnormal secondary sex determination [MP:0002212] <3>(0|2) (0|0|0)
- 1:   abnormal sexual maturation [MP:0001937] <5>(0|1) (0|0|0)
- 1:   pseudohermaphroditism [MP:0002787] <2>(0|0) (0|0|0)
- 1:   secondary sex reversal [MP:0001939](0|0) (0|0|0)


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

Family

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SCOP termFDR (all)Annotation (direct or inherited)
Extracellular domain of cell surface receptors0.0000364Direct
Nuclear receptor0.02436Inherited


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