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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