| Descriptor English: | Severe Combined Immunodeficiency | ||||||
| Descriptor Spanish: |
Inmunodeficiencia Combinada Grave
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| Descriptor Portuguese: | Imunodeficiência Combinada Severa | ||||||
| Descriptor French: | Immunodéficience combinée grave | ||||||
| Entry term(s): |
Bare Lymphocyte Syndrome Bare Lymphocyte Syndromes Combined Immunodeficiencies, Severe Combined Immunodeficiency, Severe Familial Reticuloendothelioses Familial Reticuloendotheliosis Immunodeficiencies, Severe Combined Immunodeficiency Syndrome, Severe Combined Immunodeficiency, Severe Combined Immunologic Deficiency, Severe Combined Lymphocyte Syndrome, Bare Lymphocyte Syndromes, Bare Omenn Syndrome Omenn's Syndrome Omenns Syndrome Reticuloendothelioses, Familial Reticuloendotheliosis, Familial Severe Combined Immune Deficiency Severe Combined Immunodeficiencies Severe Combined Immunodeficiency Syndrome Severe Combined Immunologic Deficiency Syndrome, Bare Lymphocyte Syndrome, Omenn Syndrome, Omenn's Syndromes, Bare Lymphocyte |
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| Tree number(s): |
C16.320.798.750 C16.614.815 C18.452.284.800 C20.673.795.750 |
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| RDF Unique Identifier: | https://id.nlm.nih.gov/mesh/D016511 | ||||||
| Scope note: | Group of rare congenital disorders characterized by impairment of both humoral and cell-mediated immunity, leukopenia, and low or absent antibody levels. It is inherited as an X-linked or autosomal recessive defect. Mutations occurring in many different genes cause human Severe Combined Immunodeficiency (SCID). |
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| Allowable Qualifiers: |
BL blood CF cerebrospinal fluid CI chemically induced CL classification CO complications DG diagnostic imaging DH diet therapy DI diagnosis DT drug therapy EC economics EH ethnology EM embryology EN enzymology EP epidemiology ET etiology GE genetics HI history IM immunology ME metabolism MI microbiology MO mortality NU nursing PA pathology PC prevention & control PP physiopathology PS parasitology PX psychology RH rehabilitation RT radiotherapy SU surgery TH therapy UR urine VE veterinary VI virology |
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| Previous Indexing: |
Immunologic Deficiency Syndromes (1974-1991) |
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| Public MeSH Note: | 1992 |
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| History Note: | 1992 |
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| Entry Version: | SEVERE COMBINED IMMUNODEFIC |
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| DeCS ID: | 29820 | ||||||
| Unique ID: | D016511 | ||||||
| Documents indexed in the Virtual Health Library (VHL): | Click here to access the VHL documents | ||||||
| Date Established: | 1992/01/01 | ||||||
| Date of Entry: | 1991/01/03 | ||||||
| Revision Date: | 2014/06/20 |
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Severe Combined Immunodeficiency
- Preferred
Bare Lymphocyte Syndrome
- Related but not broader or narrower
Omenn Syndrome
- Narrower
| Concept UI |
M0025203 |
| Scope note | Group of rare congenital disorders characterized by impairment of both humoral and cell-mediated immunity, leukopenia, and low or absent antibody levels. It is inherited as an X-linked or autosomal recessive defect. Mutations occurring in many different genes cause human Severe Combined Immunodeficiency (SCID). |
| Preferred term | Severe Combined Immunodeficiency |
| Entry term(s) |
Combined Immunodeficiencies, Severe Combined Immunodeficiency, Severe Immunodeficiencies, Severe Combined Immunodeficiency Syndrome, Severe Combined Immunodeficiency, Severe Combined Immunologic Deficiency, Severe Combined Severe Combined Immune Deficiency Severe Combined Immunodeficiencies Severe Combined Immunodeficiency Syndrome Severe Combined Immunologic Deficiency |
| Concept UI |
M0025204 |
| Preferred term | Bare Lymphocyte Syndrome |
| Entry term(s) |
Bare Lymphocyte Syndromes Lymphocyte Syndrome, Bare Lymphocyte Syndromes, Bare Syndrome, Bare Lymphocyte Syndromes, Bare Lymphocyte |
| Concept UI |
M0520254 |
| Preferred term | Omenn Syndrome |
| Entry term(s) |
Familial Reticuloendothelioses Familial Reticuloendotheliosis Omenn's Syndrome Omenns Syndrome Reticuloendothelioses, Familial Reticuloendotheliosis, Familial Syndrome, Omenn Syndrome, Omenn's |
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