Aform of combined immunodeficiency due to Calcium release activated Ca2+(CRAC) channel dysfunction characterized by recurrent infections, autoimmunity, congenital myopathy and ectodermal dysplasia. The disease is combined immunodeficiency due to STIM1 deficiency (MONDO_0013008, a Monarch Disease Ontology term). Also known as: CID due to STIM1 deficiency, immunodeficiency type 10.