Combined immunodeficiency due to ORAI1 deficiency is an ultra-rare genetic immune disorder where the body cannot move calcium properly into immune cells after ...
Dr. Nadia Falah, MD - Clinical Genetics, Genomics, Cytogenetics, Biochemical Genetics Specialist
X-linked moesin-associated immunodeficiency (often shortened to X-MAID) is a very rare, inherited immune system disease. In this condition, a change (mutation) ...
Immunodeficiency type 50 is a very rare, inherited problem of the immune system. It mainly affects T cells and B cells, which are white blood cells that fight ...
Combined immunodeficiency due to moesin deficiency is a rare, inherited immune system disease where both T cells and B cells do not work properly, so the body ...
Combined immunodeficiency due to MALT1 deficiency is a rare genetic disease where the immune system does not work properly because a gene called MALT1 is ...
Common variable immunodeficiency-8 with autoimmunity is a rare inherited immune system disease caused by harmful changes in the LRBA ...
Combined immunodeficiency due to lipopolysaccharide-responsive beige-like anchor (LRBA) protein deficiency is a rare, inherited immune system disease where ...
Combined immunodeficiency due to LRBA deficiency is a rare inherited disease where a mistake in a single gene (the LRBA gene) makes the immune system weak and ...
Combined immunodeficiency with intrauterine growth retardation–natural killer (NK) cell deficiency–neutropenia is a very rare, inherited immune system disease. ...
Combined immunodeficiency due to GINS complex subunit 1 deficiency is a very rare, inherited immune system disease. In this condition, a gene called GINS1 does ...
Combined immunodeficiency due to GINS1 deficiency is a very rare genetic disease that weakens the immune system from birth. “Combined immunodeficiency” means ...
Hyper-IgE syndrome (HIES) is a rare, inherited immune system disease where the body makes very high levels of the antibody IgE and cannot fight germs in a ...
Autosomal recessive hyper-IgE recurrent infection syndrome 2 is a rare genetic immune system disease where the body cannot fight germs properly and blood ...
Combined immunodeficiency due to dedicator of cytokinesis 8 protein deficiency is a rare, serious problem of the immune system caused by changes in a gene ...
Combined immunodeficiency due to DOCK8 deficiency is a rare, inherited disease where a gene called DOCK8 (dedicator of cytokinesis 8) does not work properly. ...
Immune dysfunction due to T-cell inactivation from a calcium entry defect is a very rare, inherited immune system disease. In this condition, T cells (a type ...
Immune dysfunction due to T-cell inactivation from a calcium entry defect is a very rare, inherited immune system disease. In this condition, T cells (a type ...
Combined immunodeficiency due to calcium release-activated calcium (CRAC) channel dysfunction is a very rare, inherited immune system disease. In this ...
Combined immunodeficiency due to CRAC channel dysfunction is a very rare inherited immune disease. In this condition, tiny calcium channels called CRAC ...
SCID-like immunodeficiency, T cell-partial, B cell-positive, NK cell-positive is a very rare primary immune system disease. Doctors also call it ...
- « Previous Page
- 1
- …
- 9
- 10
- 11
- 12
- 13
- …
- 52
- Next Page »
