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Mammalian Phenotype (MP): abnormal myeloid cell number in bone marrow

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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)
+ + + + + 5:   mammalian phenotype [MP:0000001] <29>
+ + + + 4:   hematopoietic system phenotype [MP:0005397] <2>(72|102) (78|63|30)
+ + + 3:   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 hematopoietic cell number [MP:0011180] <7>(34|57) (43|29|13)
+ + 2:   abnormal myeloid cell morphology [MP:0013658] <8>(19|41) (26|23|8)
+ + 2:   abnormal bone marrow cell morphology/development [MP:0002398] <8>(3|8) (6|6|0)
+ 1:   abnormal myeloid cell number [MP:0013661] <6>(4|7) (4|2|0)
+ 1:   abnormal bone marrow cell number [MP:0000172] <3>(0|0) (0|0|0)
0:   abnormal myeloid cell number in bone marrow [MP:0013413] <2>(0|0) (0|0|0)
- 1:   decreased myeloid cell number in bone marrow [MP:0013414](0|0) (0|0|0)
- 1:   increased myeloid cell number in bone marrow [MP:0013415](0|0) (0|0|0)