"DOID:0111971"^^ . . "A primary immunodeficiency disease characterized by onset in infancy or early childhood of recurrent infections with variable severity that has_material_basis_in homozygous or compound heterozygous mutation in CD3E on chromosome 11q23.3."^^ . _:vb50945836 . _:vb50945836 . _:vb50945836 . "CD3-epsilon deficiency"^^ . . "immunodeficiency 18"^^ . _:vb50945836 . . "disease_ontology"^^ . "OMIM:615615"^^ . _:vb50945836 . . "IMD18"^^ .