Concept information
Preferred term
Autosomal recessive SCID
Type
-
http://www.irandoc.ac.ir/onto/irandoc-meta/Concept
Narrower concepts
- Combined immunodeficiency due to CD3gamma deficiency (disorder)
- Combined immunodeficiency due to partial recombination-activating gene 1 deficiency (disorder)
- Combined immunodeficiency due to Zeta-chain associated protein kinase 70 deficiency (disorder)
- Immunodeficiency by defective expression of human leukocyte antigen class 1 (disorder)
- Immunodeficiency, short limb dwarfism syndrome
- Ligase 4 syndrome (disorder)
- Severe combined immunodeficiency due to CARD11 deficiency
- Severe combined immunodeficiency due to cytidine 5-prime triphosphate synthetase 1 deficiency
- Severe combined immunodeficiency due to deoxyribonucleic acid cross-link repair protein 1c deficiency (disorder)
- Severe combined immunodeficiency due to inhibitor of nuclear factor kappa B kinase subunit beta deficiency
- Severe combined immunodeficiency due to lymphocyte-specific protein-tyrosine kinase deficiency (disorder)
- Severe combined immunodeficiency, microcephaly, growth retardation, sensitivity to ionizing radiation syndrome (disorder)
- Severe T-cell immunodeficiency, congenital alopecia, nail dystrophy syndrome (disorder)
- T-cell negative B-cell positive severe combined immunodeficiency due to JAK3 deficiency
Finding site
Occurrence
Pathological process
In other languages
-
Persian
URI
http://www.irandoc.acir/onto/irandoc/362993009
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