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Mammalian Phenotype (MP): abnormal platelet dense granule morphology

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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:   hematopoietic system phenotype [MP:0005397] <2>(72|102) (78|63|30)
+ + + + 4:   abnormal hematopoietic system morphology/development [MP:0002396] <5>(58|86) (66|47|21)
+ + + 3:   abnormal hematopoietic cell morphology [MP:0013656] <9>(49|77) (60|43|18)
+ + 2:   abnormal blood cell morphology [MP:0013657] <4>(31|49) (37|35|14)
+ + 2:   abnormal myeloid cell morphology [MP:0013658] <8>(19|41) (26|23|8)
+ 1:   abnormal platelet morphology [MP:0004720] <6>(1|3) (2|1|0)
0:   abnormal platelet dense granule morphology [MP:0004721] <5>(0|1) (1|0|0)
- 1:   abnormal platelet ADP level [MP:0009556] <2>(0|0) (0|0|0)
- 1:   abnormal platelet ATP level [MP:0009447] <2>(0|0) (0|0|0)
- 1:   abnormal platelet calcium level [MP:0004865] <2>(0|1) (1|0|0)
- 1:   abnormal platelet serotonin level [MP:0004723] <2>(0|0) (0|0|0)
- 1:   abnormal platelet dense granule number [MP:0004722](0|0) (0|0|0)


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Family

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SCOP termFDR (all)Annotation (direct or inherited)
PLC-like (P variant)0.0001627Direct


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

Supra-domain (including individual superfamily)

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Supra-domain (Single) FDR (all) Annotation (direct or inherited)
C2 domain (Calcium/lipid-binding domain, CaLB)0.01429Inherited


Plot distribution on phylogenetic tree for Supra-domains (Single/Individual) annotated by this phenotype term
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