4A01.1Y Other specified combined immunodeficiencies

International Classification of Diseases for Mortality and Morbidity Statistics, 11th Revision, v2024-01

synonyms

• Other specified combined immunodeficiencies
• Combined immunodeficiency due to ORAI1 deficiency
• Combined immunodeficiency due to STIM1 deficiency
• Combined immunodeficiency T+ B+ due to partial RAG1 deficiency
• Immunodeficiency due to purine nucleoside phosphorylase deficiency
• Nucleoside phosphorylase deficiency
• deficiency of inosine phosphorylase
• deficiency of purine-nucleoside phosphorylase
• NP - [nucleoside phosphorylase] deficiency
• PNP - [purine nucleoside phosphorylase] deficiency
• Severe combined immunodeficiency - microcephaly - growth retardation - sensitivity to ionizing radiation
• Combined immunodeficiency due to Cernunnos protein deficiency
• NHEJ1 - [non-homologous end joining factor] syndrome
• DNA-ligase IV deficiency
• Ligase 4 syndrome
• LIG4 deficiency
• Combined immunodeficiency due to CRAC channel dysfunction
• Immune dysfunction due to T-cell inactivation due to calcium entry defect
• Combined immunodeficiency due to ZAP70 deficiency
• Zeta-associated-protein 70 deficiency
• Severe T-cell immunodeficiency - congenital alopecia - nail dystrophy
• SCID - [Severe combined immunodeficiency] due to winged helix deficiency
• Combined immunodeficiency due to CD3 gamma deficiency
• Familial CD8 deficiency
• Susceptibility to respiratory infections associated with CD8 alpha chain mutation
• Primary immunodeficiency with skin granulomas
• Combined cellular and humoral deficiencies and multiple granulomas
• Combined immunodeficiency due to DOCK8 deficiency
• CID - [combined immunodeficiency] due to DOCK8 - [dedicator of cytokinesis 8 protein] deficiency
• Pancytopenia due to IKZF1 mutations
• CID - [combined immunodeficiency] due to Ikaros deficiency
• X-linked immunodeficiency with magnesium defect, Epstein-Barr virus infection or neoplasia
• Combined immunodeficiency due to MAGT1 deficiency
• CID - [combined immunodeficiency] due to MAGT1 deficiency
• Hyper-IgM syndrome due to CD40 ligand deficiency
• Hyper-IgM syndrome type 1
• Hyper-IgM syndrome due to CD40L deficiency
• X-linked hyper-IgM syndrome
• HIGM1 - [hyper-IgM syndrome type 1]
• Hyper-IgM syndrome due to CD40 deficiency
• Hyper-IgM syndrome type 3
• HIGM3 - [hyper-IgM syndrome type 3]
• Combined immunodeficiency with facio-oculo-skeletal anomalies
• Corpus callosum agenesis – cataract – immunodeficiency
• Dionisi-Vici-Sabetta-Gambarara syndrome
• Vici syndrome
• Absent thumb - short stature - immune deficiency
• Hyper-IgM syndrome with susceptibility to opportunistic infections
• Hyper-IgM syndrome without susceptibility to opportunistic infections

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