Imunodeficiência Combinada Grave
Autossómica recessiva
A imunodeficiência combinada grave (SCID, na sigla em inglês) engloba um grupo de doenças monogénicas raras de imunodeficiência primária, caracterizadas pela falta de linfócitos T periféricos funcionais, o que resulta em infeções respiratórias graves de início precoce e em dificuldade de desenvolvimento. Estas doenças são classificadas de acordo com o fenótipo imunológico em SCID com ausência de células T mas presença de células B (SCID T-B+) ou SCID com ausência de ambas (SCID T-B-). Ambos estes grupos incluem várias formas, com ou sem células natural killer (NK).
Genes analisados
Também conhecida como
SCID; severe combined immunodeficiency (disease)
Inclui 51 subtipos relacionados ↓Ocultar subtipos ↑
- Cernunnos-XLF deficiency
- combined immunodeficiency due to partial RAG1 deficiency
- combined immunodeficiency with skin granulomas
- combined immunodeficiency, X-linked
- DNA ligase IV deficiency
- familial severe combined immunodeficiency
- immunodeficiency 104
- immunodeficiency 105
- immunodeficiency 18
- immunodeficiency 19
- immunodeficiency 25
- immunodeficiency 49
- immunodeficiency 73b with defective neutrophil chemotaxis and lymphopenia
- immunodeficiency 73c with defective neutrophil chemotaxis and hypogammaglobulinemia
- immunodeficiency 79
- Immunoerythromyeloid hypoplasia
- janus kinase-3 deficiency
- lung fibrosis-immunodeficiency-46,XX gonadal dysgenesis syndrome
- MHC class II deficiency
- MHC class II deficiency 1
- MHC class II deficiency 2
- MHC class II deficiency 3
- MHC class II deficiency 4
- MHC class II deficiency 5
- neutrophil immunodeficiency syndrome
- Omenn syndrome
- recombinase activating gene 1 deficiency
- recombinase activating gene 2 deficiency
- reticular dysgenesis
- reticular dysgenesis-like severe combined immunodeficiency
- severe combined immunodeficiency due to CARD11 deficiency
- severe combined immunodeficiency due to CARMIL2 deficiency
- severe combined immunodeficiency due to CD70 deficiency
- severe combined immunodeficiency due to CORO1A deficiency
- severe combined immunodeficiency due to DCLRE1C deficiency
- severe combined immunodeficiency due to DNA-PKcs deficiency
- severe combined immunodeficiency due to IKK2 deficiency
- severe combined immunodeficiency due to LAT deficiency
- severe combined immunodeficiency due to LCK deficiency
- severe combined immunodeficiency, autosomal recessive, T cell-negative, B cell-negative, NK cell-negative, due to adenosine deaminase deficiency
- severe combined immunodeficiency, autosomal recessive, T cell-negative, B cell-negative, NK cell-positive
- short-limb skeletal dysplasia with severe combined immunodeficiency
- T-B- severe combined immunodeficiency
- T-B+ severe combined immunodeficiency
- T-B+ severe combined immunodeficiency due to CD3delta/CD3epsilon/CD3zeta
- T-B+ severe combined immunodeficiency due to CD45 deficiency
- T-B+ severe combined immunodeficiency due to gamma chain deficiency
- T-B+ severe combined immunodeficiency due to IL-7Ralpha deficiency
- T-B+ severe combined immunodeficiency due to JAK3 deficiency
- T-cell immunodeficiency, congenital alopecia, and nail dystrophy
- T+ B+ severe combined immunodeficiency
