- congenital immunodeficiency
- врождённый иммунодефицит
Англо-русский словарь по иммунологии и иммуногенетике. — М.: Русский язык. Сучков С. В. Под ред. акад. Р. В. Петрова. 1990.
Англо-русский словарь по иммунологии и иммуногенетике. — М.: Русский язык. Сучков С. В. Под ред. акад. Р. В. Петрова. 1990.
congenital disorder — Structural abnormality (e.g., atresia, agenesis), functional problem (e.g., cystic fibrosis, phenylketonuria), or disease present at birth. Almost all are due to genetic factors (inherited or spontaneous mutations, chromosomal disorders),… … Universalium
Congenital disorder of glycosylation type IIc — Classification and external resources OMIM 266265 Congenital disorder of glycosylation type IIc or Leukocyte adhesion deficiency 2 (LAD2) is a type of leukocyte adhesion deficiency attributable to the absence of neutrophil sialyl LewisX, a ligand … Wikipedia
Congenital hypothyroidism — Classification and external resources ICD 10 E00, E03.0, E03.1 … Wikipedia
Congenital disorder — Classification and external resources MeSH D009358 … Wikipedia
Congenital abnormality — Congenital Anomaly Classification and external resources ICD 10 Chapter Q MeSH D000013 … Wikipedia
Congenital rubella syndrome — Classification and external resources Congenital Cataracts (white pupils) due to congenital rubella syndrome ICD … Wikipedia
Congenital syphilis — Classification and external resources Notched incisors known as Hutchinson s teeth which are characteristic of congenital syphilis ICD … Wikipedia
Congenital cytomegalovirus infection — Classification and external resources Micrograph of a cytomegalovirus (CMV) infection of the placenta (CMV placentitis). The characteristic large nucleus of a CMV infected cell is seen off centre at the bo … Wikipedia
Congenital insensitivity to pain with anhidrosis — Classification and external resources OMIM 256800 DiseasesDB 32097 MeSH … Wikipedia
Congenital amegakaryocytic thrombocytopenia — Classification and external resources ICD 9 287.33, 287.5 OMIM … Wikipedia
Congenital generalized lipodystrophy — Classification and external resources eMedicine article/1113171 Congenital generalized lipodystrophy (also known as Berardinelli–Seip syndrome) is a rare autosomal dominant skin condition, characterized by an extreme paucity of fat in the… … Wikipedia