Noun:

తీవ్రమైన ఉమ్మడి రోగ నిరోధక,

severe combined immunodeficiency's Usage Examples:

ERT has also been used to treat patients with severe combined immunodeficiency (SCID) resulting from an adenosine deaminase deficiency (ADA-SCID).

gene can cause dysfunction of the kinase leading to autosomal severe combined immunodeficiency (SCID) disease or on the contrary, the activation of mutated.

Omenn syndrome is an autosomal recessive severe combined immunodeficiency.

In 1972, Giblett received samples from a patient with severe combined immunodeficiency disease (SCID).

The severe combined immunodeficiency (SCID) is a severe immunodeficiency genetic disorder that is characterized by the complete inability of the adaptive.

under the brand name Strimvelis, is a medication used to treat severe combined immunodeficiency due to adenosine deaminase deficiency (ADA-SCID).

of immune cell is affected, this disease is classified as a severe combined immunodeficiency disease (SCID).

Omenn syndrome is a severe combined immunodeficiency disease characterized by skin rash, slenomegaly, and lymphadenopathy.

Deficiency in this enzyme causes a form of severe combined immunodeficiency disease (SCID), in which there is dysfunction of both B and T lymphocytes.

syndrome, ataxia telangiectasia, the radiosensitive forms of severe combined immunodeficiency disease (SCID), the autoimmune lymphoproliferative syndrome, and.

It is a form of severe combined immunodeficiency.

was critically ill with adenosine deaminase deficiency severe combined immunodeficiency disease (ADA SCID).

Mutations that abrogate Jak3 functions cause an autosomal severe combined immunodeficiency disease (SCID) while activating Jak3 mutations lead to the development.

Synonyms:

severe combined immunodeficiency disease, X-linked SCID, monogenic disease, ADA-SCID, immunodeficiency, SCID, monogenic disorder, X-SCID,

Antonyms:

immunocompetence, ability,