Concept information
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Genetic Diseases, Inborn
Primary Immunodeficiency Diseases
Severe Combined Immunodeficiency
Immune System Diseases
Immunologic Deficiency Syndromes
Primary Immunodeficiency Diseases
Severe Combined Immunodeficiency
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Infant, Newborn, Diseases
Severe Combined Immunodeficiency
Término preferido
X-Linked Combined Immunodeficiency Diseases
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Tipo
-
mesh:Descriptor
Definición
- Forms of combined immunodeficiency caused by mutations in the gene for INTERLEUKIN RECEPTOR COMMON GAMMA SUBUNIT. Both severe and non-severe subtypes of the disease have been identified.
Concepto genérico
Etiquetas alternativas
- Combined Immunodeficiency, X-Linked
- Immunodeficiency 4
- Immunodeficiency 6
- Immunodeficiency Diseases, X-Linked Combined
- SCID, X-Linked
- SCIDX
- SCIDX1
- Severe Combined Immunodeficiency, X-Linked
- Severe Combined Immunodeficiency, X-Linked, T Cell Negative, B Cell Positive, NK Cell Negative
- Severe Combined Immunodeficiency, X-Linked, T Cell-Negative, B Cell-Positive, NK Cell-Negative
- X-Linked Combined Immunodeficiency
- X-Linked Immunodeficiency Disease
- X-Linked Immunodeficiency Syndrome
- X-Linked SCID
- X-Linked Severe Combined Immunodeficiency
- X-SCID
- XSCID
En otras lenguas
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francés
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Déficits immunitaires combinés liés à l'X
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Déficits immunitaires combinés sévères liés à l'X
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DICS liés à l'X
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DICS-X
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Maladies immunitaires combinées graves liées à l'X
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Maladies immunitaires combinées sévères liées à l'X
URI
http://data.loterre.fr/ark:/67375/JVR-SC1LJ8FN-N
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