WormMine

WS295

Intermine data mining platform for C. elegans and related nematodes

Ontology Relation :

Relationship  is_a Parent Term . Identifier  DOID:612
Child Term . Identifier  DOID:0081150 Direct  false
Redundant  false
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1 Child Term

Identifier Name Description
DOID:0081150 common variable immunodeficiency 7 A common variable immunodeficiency that has_material_basis_in compound heterozygous mutation in the CD21 gene (CR2) on chromosome 1q32.

1 Parent Term

Identifier Name Description
DOID:612 primary immunodeficiency disease An immune system disease that results when one or more essential parts of the immune system is missing or not working properly at birth due to a genetic mutation.