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Mammalian Phenotype (MP): abnormal intramembranous bone ossification

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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:   mammalian phenotype [MP:0000001] <29>
+ + + 3:   skeleton phenotype [MP:0005390] <2>(46|63) (50|41|26)
+ + 2:   abnormal skeleton physiology [MP:0001533] <12>(17|20) (18|12|6)
+ 1:   abnormal bone ossification [MP:0008271] <10>(8|11) (8|1|2)
0:   abnormal intramembranous bone ossification [MP:0008273] <4>(0|0) (0|0|1)
- 1:   delayed intramembranous bone ossification [MP:0003420] <1>(0|0) (0|0|0)
- 1:   premature intramembranous bone ossification [MP:0003418] <1>(0|0) (0|0|0)
- 1:   failure of intramembranous bone ossification [MP:0008276](0|0) (0|0|0)
- 1:   impaired ossification of basisphenoid bone [MP:0000105](0|0) (0|0|0)

Supra-domain (Single|Duplex|Triple)

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Supra-domain (Triple) in N- to C-terminal order

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Supra-domain (Triple) in N- to C-terminal order FDR (all) Annotation (direct or inherited)
48726,48726,48726
  • 48726 - Immunoglobulin
  • 48726 - Immunoglobulin
  • 48726 - Immunoglobulin
  • 0.0006Direct

    LINKTO: Supra-domain2BO Download and Supra-domain2BO Algorithm