Term Name: immunodeficiency 58
Synonyms: IMD58, severe combined immunodeficiency due to CARMIL2 deficiency
Definition: A combined T cell and B cell immunodeficiency characterized by defective T-cell function with decreased Treg cells and deficient CD3/CD28 costimulation responses in both CD4+ and CD8+ T cells, variable impairment in B-cell function, early-onset skin lesions, recurrent respiratory infections or allergies, and chronic persistent infections that has_material_basis_in homozygous or compound heterozygous mutation in the CARMIL2 gene on chromosome 16q22.1.
Ontology: Human Disease [DOID:0111984]   ( DOID:0111984 )

Relationships
is a type of: autosomal recessive disease combined T cell and B cell immunodeficiency