Condition
Severe Combined Immunodeficiency
General Healthcare
Overview
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).
This information is general and should not be treated as medical advice. Always speak directly with a qualified healthcare professional before making decisions about treatment, diagnosis, procedures, medicines or care.
Quick facts about Severe Combined Immunodeficiency
- Topic type
- Condition
- Category
- General Healthcare
- MeSH classification
- C16.320.798.750|C16.614.815|C18.452.284.800|C20.673.795.750
Preparing for an appointment about Severe Combined Immunodeficiency
If you are speaking with a healthcare professional about Severe Combined Immunodeficiency, it can help to prepare a few details in advance.
- Write down your symptoms and when they started.
- Bring details of any medicines, supplements or previous treatments.
- Ask what tests or assessments may be needed.
- Ask what treatment or management options may be suitable.
- Ask when you should seek urgent medical help or follow-up care.
Finding care related to Severe Combined Immunodeficiency
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Source: Medical Subject Headings (MeSH), produced by the U.S. National Library of Medicine. EuroCareFinder is not endorsed by the National Library of Medicine. MeSH version: 2026.