Syndromic agammaglobulinemia
MONDO:0016463A agammaglobulinemia that is part of a larger syndrome.
Also known as: hypogammaglobulinemia, syndrome associated with agammaglobulinemia, syndromic agammaglobulinemia, syndromic hypogammaglobulinemia
74 clinical trials for this condition and its sub-types, 7 tagged with Syndromic agammaglobulinemia itself.
Follow this condition to get notified about new trialsWhere it sits in the disease tree
Browse by category →Sub-types of Syndromic agammaglobulinemia
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Common variable immunodeficiency 29 trials · 31 incl. sub-types
16 sub-types
- Immunodeficiency, common variable, 12 1 trial
- Pancytopenia due to IKZF1 mutations 1 trial
- IL21-related infantile inflammatory bowel disease 0 trials
- Combined immunodeficiency due to LRBA deficiency 0 trials
- Immune deficiency, familial variable 0 trials
- Immunodeficiency, common variable, 1 0 trials
- Immunodeficiency, common variable, 10 0 trials Sub-types →
- Immunodeficiency, common variable, 14 0 trials
- Immunodeficiency, common variable, 15 0 trials
- Immunodeficiency, common variable, 2 0 trials
- Immunodeficiency, common variable, 3 0 trials
- Immunodeficiency, common variable, 4 0 trials
- Immunodeficiency, common variable, 5 0 trials
- Immunodeficiency, common variable, 6 0 trials
- Immunodeficiency, common variable, 7 0 trials
- Immunodeficiency, common variable, due to APRIL deficiency 0 trials
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Transient hypogammaglobulinemia 0 trials
1 sub-type