Also known as:
Athabaskan Severe combined immunodeficiency, DCLRE1C severe combined immunodeficiency (disease), RS-SCID, SCID due to ARTEMIS deficiency, SCID due to DCLRE1C deficiency, SCID due to artemis deficiency, SCID, Athabascan type, SCID, Athabaskan type, SCID, autosomal recessive, T cell-negative, B cell-negative, NK cell-positive, with sensitivity to ionising radiation, SCID, autosomal recessive, T cell-negative, B cell-negative, NK cell-positive, with sensitivity to ionizing radiation, artemis deficiency, severe combined immunodeficiency (disease) caused by mutation in DCLRE1C, severe combined immunodeficiency due to ARTEMIS deficiency, severe combined immunodeficiency due to DCLRE1C deficiency, severe combined immunodeficiency due to artemis deficiency, severe combined immunodeficiency with sensitivity to ionising radiation, severe combined immunodeficiency with sensitivity to ionizing radiation, severe combined immunodeficiency, Athabascan type, severe combined immunodeficiency, Athabaskan type, severe combined immunodeficiency, Athabaskan-type, severe combined immunodeficiency, partial
Also known as:
IMD26, SCID due to DNA-PKcs deficiency, immunodeficiency 26 with or without neurologic abnormalities, immunodeficiency 26, with or without neurologic abnormalities
Also known as:
IMD15, SCID due to IKK2 deficiency, immunodeficiency 15, immunodeficiency 15B, immunodeficiency type 15
Also known as:
IMD52, SCID due to LAT deficiency, immunodeficiency 52
Also known as:
IMD22, SCID due to LCK deficiency, SCID due to lymphocyte-specific protein tyrosine kinase deficiency, immunodeficiency 22, immunodeficiency type 22, severe combined immunodeficiency due to lymphocyte-specific protein tyrosine kinase deficiency
Also known as:
ADA, ADA deficiency, ADA-SCID, SCID due to ADA deficiency, SCID due to ADA deficiency, delayed onset, SCID due to ADA deficiency, early-onset, SCID due to ADA deficiency, late-onset, SCID due to adenosine deaminase deficiency, adenosine deaminase deficiency, adenosine deaminase deficiency, partial, adenosine deaminase deficiency, partial, Autosomal recessive, Somatic mosaicism, adenosine deaminase deficient severe combined immunodeficiency, partial ADA deficiency, severe combined immunodeficiency due to ADA deficiency, severe combined immunodeficiency due to ADA deficiency, Autosomal recessive, Somatic mosaicism, severe combined immunodeficiency due to adenosine deaminase deficiency, severe combined immunodeficiency, autosomal recessive, T cell-negative, B cell-negative, NK cell-negative, due to adenosine deaminase deficiency
Also known as:
SCID due to complete RAG1-2 deficiency, SCID due to complete RAG1/2 deficiency, SCID, AR, T-cell negative, B-cell negative, NK cell-positive, SCID, T cell-negative, B cell-negative, NK cell-positive, severe combined immunodeficiency due to complete RAG1-2 deficiency, severe combined immunodeficiency due to complete RAG1/2 deficiency, severe combined immunodeficiency, B cell-negative, severe combined immunodeficiency, autosomal recessive, T cell-negative, B cell-negative, NK cell-positive, severe immunodeficiency, autosomal recessive, T-cell negative, B-cell negative, NK cell-positive
Also known as:
AHMIO2, anemia, hypochromic microcytic, with iron overload 2, anemia, hypochromic microcytic, with iron overload type 2, severe congenital hypochromic sideroblastic anaemia, severe congenital hypochromic sideroblastic anemia
Also known as:
severe congenital (neonatal) NM
