← Back to Conditions

Autosomal recessive severe combined immunodeficiency disease

disorder
SNOMED 362993009CUI C0259743

Overview

Autosomal recessive severe combined immunodeficiency disease is a disorder.

Auto-generated from clinical reference data. Not a substitute for medical advice.

Related Conditions

Adenosine deaminase deficiency(child)
Severe combined immunodeficiency due to deoxyribonucleic acid cross-link repair protein 1c deficiency(child)
Combined immunodeficiency due to Zeta-chain associated protein kinase 70 deficiency(child)
T-cell negative B-cell positive severe combined immunodeficiency due to JAK3 deficiency(child)
Severe combined immunodeficiency, microcephaly, growth retardation, sensitivity to ionizing radiation syndrome(child)
Lung fibrosis, immunodeficiency, 46,XX gonadal dysgenesis syndrome(child)
Severe T-cell immunodeficiency, congenital alopecia, nail dystrophy syndrome(child)
Severe combined immunodeficiency with hypereosinophilia(child)
Hepatic veno-occlusive disease with immunodeficiency syndrome(child)
LIG4 syndrome(child)
Combined immunodeficiency due to CD3gamma deficiency(child)
Combined immunodeficiency due to partial RAG1 deficiency(child)
Severe combined immunodeficiency due to cytidine 5-prime triphosphate synthetase 1 deficiency(child)
Severe combined immunodeficiency due to inhibitor of nuclear factor kappa B kinase subunit beta deficiency(child)
Severe combined immunodeficiency due to LCK (lymphocyte-specific protein-tyrosine kinase) deficiency(child)
Immunodeficiency, short limb dwarfism syndrome(child)
Severe combined immunodeficiency due to LAT (linker for activation of T cells) deficiency(child)
Autosomal recessive T-cell negative, B-cell positive severe combined immunodeficiency due to interleukin 7 receptor deficiency(child)
Autosomal recessive T-cell negative, B-cell positive severe combined immunodeficiency due to protein tyrosine phosphatase receptor type C deficiency(child)
Severe combined immunodeficiency due to CORO1A deficiency(child)

Quick Facts

SNOMED CT
362993009
UMLS CUI
C0259743
Fully Specified Name
Autosomal recessive severe combined immunodeficiency disease (disorder)
Specialists
0
Diagnostic Biomarkers
0
Medical Disclaimer

This information is for educational purposes only and does not constitute medical advice, diagnosis, or treatment. Always consult with a qualified healthcare provider regarding any medical condition or treatment plan.

Clinical content is derived from the SNOMED CT clinical ontology and curated medical knowledge graphs.