DO_rare_slim has material basis in autosomal recessive disease T cell and NK cell immunodeficiency immunodeficiency 10 MIM:612783 CID due to STIM1 deficiency disease_ontology A T cell and NK cell immunodeficiency characterized by onset in childhood of recurrent infections due to defective T- and NK-cell function that has_material_basis_in homozygous mutation in the STIM1 gene on chromosome 11p15.4. IMD10 ORDO:317430 UMLS_CUI:C2748557 DOID:0111970 MESH:C557827 STIM1 deficiency combined immunodeficiency due to STIM1 deficiency immune dysfunction with T-cell inactivation due to calcium entry defect 2 autosomal recessive inheritance