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Mammalian Phenotype (MP): mammalian phenotype

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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)
0:   mammalian phenotype [MP:0000001] <29>
- 1:   pigmentation phenotype [MP:0001186] <13>(4|5) (5|1|3)
- 1:   growth/size/body region phenotype [MP:0005378] <12>(65|96) (72|47|25)
- 1:   embryo phenotype [MP:0005380] <7>(43|55) (47|28|19)
- 1:   homeostasis/metabolism phenotype [MP:0005376] <7>(139|174) (149|96|44)
- 1:   cellular phenotype [MP:0005384] <6>(97|118) (104|57|31)
- 1:   integument phenotype [MP:0010771] <5>(46|64) (52|34|18)
- 1:   mortality/aging [MP:0010768] <4>(82|115) (89|69|51)
- 1:   taste/olfaction phenotype [MP:0005394] <4>(4|4) (4|0|0)
- 1:   adipose tissue phenotype [MP:0005375] <2>(16|24) (18|10|5)
- 1:   cardiovascular system phenotype [MP:0005385] <2>(67|85) (78|57|35)
- 1:   digestive/alimentary phenotype [MP:0005381] <2>(38|46) (40|19|9)
- 1:   endocrine/exocrine gland phenotype [MP:0005379] <2>(50|79) (55|35|12)
- 1:   hearing/vestibular/ear phenotype [MP:0005377] <2>(21|24) (24|14|5)
- 1:   hematopoietic system phenotype [MP:0005397] <2>(72|102) (78|63|30)
- 1:   immune system phenotype [MP:0005387] <2>(77|115) (87|66|35)
- 1:   limbs/digits/tail phenotype [MP:0005371] <2>(18|26) (21|22|18)
- 1:   liver/biliary system phenotype [MP:0005370] <2>(38|39) (41|19|10)
- 1:   muscle phenotype [MP:0005369] <2>(48|56) (54|37|28)
- 1:   neoplasm [MP:0002006] <2>(32|37) (38|18|7)
- 1:   nervous system phenotype [MP:0003631] <2>(99|129) (113|80|50)
- 1:   normal phenotype [MP:0002873] <2>(8|12) (8|4|5)
- 1:   renal/urinary system phenotype [MP:0005367] <2>(41|47) (46|26|12)
- 1:   reproductive system phenotype [MP:0005389] <2>(37|56) (46|17|6)
- 1:   respiratory system phenotype [MP:0005388] <2>(33|46) (37|29|15)
- 1:   skeleton phenotype [MP:0005390] <2>(45|63) (49|42|26)
- 1:   vision/eye phenotype [MP:0005391] <2>(44|54) (51|27|17)
- 1:   behavior/neurological phenotype [MP:0005386] <1>(38|61) (43|40|24)
- 1:   craniofacial phenotype [MP:0005382] <1>(20|36) (24|18|10)
- 1:   no phenotypic analysis [MP:0003012](0|0) (0|0|0)