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Disease Ontology (DO): metal metabolism disorder

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Root: DO Hierarchy (disease ontology from University of Maryland)

Shortest distance to current term (+ for parents, - for children) DO term [DO ID] <#Children> (#SF|#FA) #Supra-domain
(Single|Duplex|Triple)
+ + + 3:   disease [DOID:4] <8>
+ + 2:   disease of metabolism [DOID:0014667] <2>(22|34) (27|12|5)
+ 1:   inherited metabolic disorder [DOID:655] <18>(12|15) (16|5|0)
0:   metal metabolism disorder [DOID:896] <8>(2|2) (2|1|0)
- 1:   hemochromatosis [DOID:2352] <6>(1|2) (1|1|0)
- 1:   primary hypomagnesemia [DOID:0060879] <6>(0|0) (0|0|0)
- 1:   familial periodic paralysis [DOID:1029] <2>(1|0) (1|0|0)
- 1:   pseudohypoparathyroidism [DOID:4184] <2>(0|0) (0|0|0)
- 1:   Menkes disease [DOID:1838](0|0) (0|0|0)
- 1:   Wilson disease [DOID:893](0|0) (0|0|0)
- 1:   acrodermatitis enteropathica [DOID:0050605](0|0) (0|0|0)
- 1:   atransferrinemia [DOID:0050649](0|0) (0|0|0)


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Superfamily

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SCOP termFDR (all)Annotation (direct or inherited)
MHC antigen-recognition domain0.001067Inherited
Voltage-gated potassium channels0.003508Inherited


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Family

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SCOP termFDR (all)Annotation (direct or inherited)
C1 set domains (antibody constant domain-like)0.00008422Direct
MHC antigen-recognition domain0.0006255Direct


Plot distribution on phylogenetic tree for Superfamily and/or Family domains annotated by this phenotype term
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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)
MHC antigen-recognition domain0.0006734Direct
Voltage-gated potassium channels0.002344Inherited

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Supra-domain (Duplex) in N- to C-terminal order FDR (all) Annotation (direct or inherited)
54452,48726
  • 54452 - MHC antigen-recognition domain
  • 48726 - Immunoglobulin
  • 0.0006734Direct


    Plot distribution on phylogenetic tree for Supra-domains (Single/Individual) annotated by this phenotype term
    Plot tree as:   Download Newick format tree:
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