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Disease Ontology (DO): combined T cell and B cell immunodeficiency

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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)
+ + + + 4:   disease [DOID:4] <8>
+ + + 3:   disease of anatomical entity [DOID:7] <12>(143|187) (147|103|58)
+ + 2:   immune system disease [DOID:2914] <4>(39|47) (42|27|16)
+ 1:   primary immunodeficiency disease [DOID:612] <8>(6|3) (6|3|0)
0:   combined T cell and B cell immunodeficiency [DOID:628] <5>(0|1) (0|1|0)
- 1:   severe combined immunodeficiency [DOID:627] <21>(0|1) (0|1|0)
- 1:   CD40 deficiency [DOID:0060023](0|0) (0|0|0)
- 1:   CD40 ligand deficiency [DOID:0060022](0|0) (0|0|0)
- 1:   DNA ligase IV deficiency [DOID:0060021](0|0) (0|0|0)
- 1:   purine nucleoside phosphorylase deficiency [DOID:5813](0|0) (0|0|0)


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Family

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SCOP termFDR (all)Annotation (direct or inherited)
C1 set domains (antibody constant domain-like)0.02506Inherited


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 (Duplex) in N- to C-terminal order FDR (all) Annotation (direct or inherited)
55550,56112
  • 55550 - SH2 domain
  • 56112 - Protein kinase-like (PK-like)
  • 0.06761Inherited