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Mammalian Phenotype (MP): white spotting

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

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:   integument phenotype [MP:0010771] <5>(46|64) (53|34|18)
+ + + + 4:   abnormal skin adnexa morphology [MP:0010678] <12>(21|28) (23|21|10)
+ + + 3:   abnormal coat/ hair morphology [MP:0000367] <7>(8|9) (10|5|4)
+ + 2:   abnormal coat appearance [MP:0001510] <11>(8|9) (10|5|4)
+ + 2:   pigmentation phenotype [MP:0001186] <13>(4|5) (6|1|3)
+ 1:   abnormal coat/hair pigmentation [MP:0002075] <20>(3|3) (3|0|2)
0:   white spotting [MP:0002938] <3>(0|1) (0|0|0)
- 1:   belly spot [MP:0000373](0|0) (0|0|0)
- 1:   head spot [MP:0002939](0|0) (0|0|0)
- 1:   variable body spotting [MP:0002940](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)
Paired domain0.000003529Direct


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