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Mammalian Phenotype (MP): abnormal ear pigmentation

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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> #Domains
(Superfamily|Family)
#Supra-domain
(Single|Duplex|Triple)
+ + + + 4:   integument phenotype [MP:0010771] <5>(46|64) (53|34|18)
+ + + + 4:   mammalian phenotype [MP:0000001] <29>
+ + + 3:   hearing/vestibular/ear phenotype [MP:0005377] <2>(20|24) (23|14|5)
+ + + 3:   abnormal skin morphology [MP:0002060] <16>(19|26) (24|13|8)
+ + + 3:   growth/size/body region phenotype [MP:0005378] <12>(64|95) (71|47|27)
+ + + 3:   craniofacial phenotype [MP:0005382] <1>(20|36) (24|17|10)
+ + 2:   abnormal head morphology [MP:0000432] <8>(12|23) (14|5|2)
+ + 2:   pigmentation phenotype [MP:0001186] <13>(4|5) (6|1|3)
+ + 2:   abnormal ear morphology [MP:0002102] <4>(16|21) (18|14|5)
+ + 2:   abnormal craniofacial morphology [MP:0000428] <5>(20|36) (24|17|10)
+ + 2:   abnormal skin coloration [MP:0011239] <1>(0|0) (1|1|0)
+ 1:   abnormal skin pigmentation [MP:0002095] <11>(0|0) (1|1|0)
+ 1:   abnormal outer ear morphology [MP:0002177] <19>(0|1) (1|1|0)
0:   abnormal ear pigmentation [MP:0000015] <2>(0|0) (0|0|0)
- 1:   decreased ear pigmentation [MP:0011279](0|0) (0|0|0)
- 1:   increased ear pigmentation [MP:0011278](0|0) (0|0|0)