Genetic immunologic deficiency diseases and syndromes due to mutations in genes involved in IMMUNITY generally characterized by an increased susceptibility to infectious diseases. They are often associated with AUTOIMMUNE DISEASE manifestations.

Synonyms: Primary Antibody Deficiency, Congenital Immunodeficiency Syndrome, Primary Antibody Deficiency Syndromes, Primary Immunodeficiency Syndrome, Primary Antibody Deficiency Disorder, Inherited Immunodeficiency Syndrome, Congenital Immunodeficiency Disorders, Inherited Immunodeficiency Disease, Congenital Immunodeficiency Syndromes, Inherited Immunodeficiency Syndromes, Primary Immune Deficiency Disorder, Immunodeficiency Diseases, Inherited, Inherited Immunodeficiency Disorders, Immunodeficiency Disorder, Congenital, Immunodeficiency Disease, Congenital, Primary Antibody Deficiency Disorders, Immunodeficiency Syndromes, Congenital, Primary Immunodeficiency Diseases, Immune Deficiency, Primary, Primary Immune Deficiency Syndromes, Immunodeficiency Disease, Inherited, Primary Immune Deficiency Diseases, Immunodeficiency Disorders, Inherited, Immunodeficiency Disorder, Inherited, Immunodeficiency Diseases, Primary, Primary Immune Deficiencies, Primary Immune Deficiency Disease, Primary Immunodeficiency Disorder, Primary Immunodeficiency Syndromes, Immunodeficiency Disorders, Congenital, Congenital Immunodeficiency Disorder, Immunodeficiency Syndromes, Primary, Primary Antibody Deficiency Syndrome, Immunodeficiency Syndrome, Inherited, Inherited Immunodeficiency Diseases, Inherited Immunodeficiency Disorder, Immunodeficiency Diseases, Congenital, Congenital Immunodeficiency Disease, Immunodeficiency Syndrome, Primary, Immunodeficiency Syndromes, Inherited, Primary Immunodeficiency Disorders, Immunodeficiency Disorder, Primary, Deficiency, Primary Immune, Primary Immunodeficiency Disease, Antibody Deficiency, Primary, Primary Antibody Deficiencies, Congenital Immunodeficiency Diseases, Primary Immune Deficiency, Primary Immune Deficiency Disorders, Primary Immune Deficiency Syndrome, Immunodeficiency Disease, Primary, Immunodeficiency Syndrome, Congenital

Instance information

comment

2020

identifier

D000081207