- blood sugar deficiency
- Медицина: недостаток сахара в крови
Универсальный англо-русский словарь. Академик.ру. 2011.
blood sugar deficiency
Смотреть что такое "blood sugar deficiency" в других словарях:
blood — bloodlike, adj. /blud/, n. 1. the fluid that circulates in the principal vascular system of human beings and other vertebrates, in humans consisting of plasma in which the red blood cells, white blood cells, and platelets are suspended. 2. the… … Universalium
blood disease — Introduction any disease of the blood, involving the red blood cells (erythrocytes (erythrocyte)), white blood cells (leukocytes (leukocyte)), or platelets (platelet) (thrombocytes) or the tissues in which these elements are formed the bone … Universalium
Deficiency, GALT — Lack of the enzyme called GALT (galactose 1 phosphate uridyl transferase) which causes the genetic metabolic disease galactosemia, one of the diseases in many newborn screening panels. The disease can be fatal, if undetected. If detected, it can… … Medical dictionary
Sugar Ray Robinson — Statistics Real name Walker Smith Jr. Nickname(s) Sugar Rated at Lightweight Welterweight … Wikipedia
Malonyl-CoA decarboxylase deficiency — Classification and external resources Malonyl CoA OMIM 248360 … Wikipedia
GALT deficiency — Lack of the enzyme called GALT (galactose 1 phosphate uridyl transferase) which causes the genetic metabolic disease galactosemia, one of the diseases in many newborn screening panels. The disease can be fatal, if undetected. If detected, it can… … Medical dictionary
Mitochondrial trifunctional protein deficiency — Classification and external resources OMIM 609015 DiseasesDB 34111 eMedi … Wikipedia
3-hydroxy-3-methylglutaryl-CoA lyase deficiency — Infobox Disease Name = PAGENAME Caption = HMG CoA DiseasesDB = 29826 ICD10 = ICD9 = ICDO = OMIM = 246450 MedlinePlus = eMedicineSubj = eMedicineTopic = MeshID = C0080473 hydroxy 3 methylglutaryl CoA lyase deficiency also referred to as HMG CoA… … Wikipedia
Carnitine-acylcarnitine translocase deficiency — DiseaseDisorder infobox Name = Carnitine acylcarnitine translocase deficiency ICD10 = ICD9 = ICD9|272.8 Carnitine acylcarnitine translocase deficiency is a rare, autosomal recessive metabolic disorder that prevents the body from converting long… … Wikipedia
Carnitine palmitoyltransferase II deficiency — Classification and external resources Carnitine ICD 9 … Wikipedia
Systemic primary carnitine deficiency — CUD is an acronym sometimes used for primary carnitine deficiency. For other uses, see Cud (disambiguation). Systemic primary carnitine deficiency Classification and external resources Carnitine … Wikipedia
