Immunodeficiency associated with chromosomal abnormality

Immunodeficiency associated with chromosomal abnormality (disorder)

active

Code	`234632005`
Semantic tag	disorder
Module	international
Definition	primitive
Effective time	20020131

Parents (1)

58606001Primary immune deficiency disorder disorder

Children (21)

68504005Ataxia-telangiectasia syndrome disorder
722288007Autoimmune enteropathy and endocrinopathy with susceptibility to chronic infection syndrome disorder
722290008Autoimmune lymphoproliferative syndrome with recurrent viral infection disorder
4434006Bloom syndrome disorder
234633000Centromeric instability of chromosomes 1,9 and 16 and immunodeficiency disorder
234634006Chromosome 18 syndromes and antibody deficiency disorder
234635007Chromosome 22 abnormalities with hypogammaglobulinaemia disorder
766879006Combined immunodeficiency due to OX40 deficiency disorder
765327005Congenital sideroblastic anaemia, B-cell immunodeficiency, periodic fever, developmental delay syndrome disorder
234637004Deletion of X-chromosome and hypogammaglobulinaemia disorder
723334006FADD-related immunodeficiency disorder
763713000Idiopathic CD4 lymphocytopenia disorder
234640004Immunodeficiency associated with 18p syndrome disorder
766705006Immunodeficiency due to ficolin 3 deficiency disorder
234638009Microcephaly, normal intelligence and immunodeficiency disorder
723443003Neutrophil immunodeficiency syndrome disorder
718717004Primary immunodeficiency syndrome due to p14 deficiency disorder
724275005Primary immunodeficiency with natural killer cell deficiency and adrenal insufficiency disorder
723508002RAS-associated autoimmune leucoproliferative disease disorder
234639001Triple X syndrome, epilepsy, and hypogammaglobulinaemia disorder
724276006X-linked immune dysregulation, polyendocrinopathy, enteropathy syndrome disorder