- base deficiency
- 碱缺失
Medical Chinese dictionary (湘雅医学词典). 2013.
base deficiency
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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
Deficiency, UROD — Lack of the enzyme uroporphyrinogen decarboxylase (UROD) which is the basic cause of porphyria cutanea tarda (PCT), the late skin form of porphyria. PCT is a genetic photosensitive (light sensitive) skin disease with onset in adult life with a… … Medical dictionary
Deficiency, uroporphyrinogen decarboxylase — Lack of the enzyme uroporphyrinogen decarboxylase (UROD) which is the basic cause of porphyria cutanea tarda (PCT), the late skin form of porphyria. PCT is a genetic photosensitive (light sensitive) skin disease with onset in adult life with a… … Medical dictionary
Congenital adrenal hyperplasia due to 21-hydroxylase deficiency — Classification and external resources Deficient 21 Hydroxylase can lead to accumulation of 17 Hydroxyprogesterone ICD … Wikipedia
Carnitine palmitoyltransferase II deficiency — Classification and external resources Carnitine ICD 9 … Wikipedia
N-Acetylglutamate synthase deficiency — Classification and external resources N Acetylglutamic acid OMIM 237310 … Wikipedia
Adenylosuccinate lyase deficiency — Infobox Disease Name = PAGENAME Caption = DiseasesDB = 33422 ICD10 = ICD9 = ICDO = OMIM = 103050 MedlinePlus = eMedicineSubj = eMedicineTopic = MeshID = Adenylosuccinate lyase deficiency, also called adenylosuccinase deficiency, [OMIM|103050] is… … Wikipedia
DNA repair-deficiency disorder — Classification and external resources MeSH D049914 A DNA repair deficiency disorder is a medical condition due to reduced functionality of DNA repair. DNA repair defects are seen in nearly all of the diseases described as accelerated aging… … Wikipedia
Aldolase A deficiency — Infobox Disease Name = PAGENAME Caption = DiseasesDB = 29873 ICD10 = ICD9 = ICDO = OMIM = 611881 MedlinePlus = eMedicineSubj = eMedicineTopic = MeshID = Aldolase A deficiency, also called ALDOA deficiency and red cell aldolase deficiency,… … Wikipedia
acid–base reaction — ▪ chemistry Introduction a type of chemical process typified by the exchange of one or more hydrogen ions, H+, between species that may be neutral (molecules, such as water, H2O; or acetic acid, CH3CO2H) or electrically charged (ions, such… … Universalium
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
