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Addison-Schilder
Adrenoleukodystrophy
Amylopectinosis
Amylopectinosis brancher deficiency
Andersen disease
Andersen's disease
Brancher deficiency
Brancher enzyme deficiency
Carnitin
Carnitine
Carnitine deficiency
Carnitine palmitoyltransferase II deficiency
Deficiency
Familia
GSD IV
Glycogen storage disease type IV
Glycogenosis IV
Hexokinase deficiency
Muscle carnitine palmityltransferase deficiency
Najjar-Andersen syndrome
PK
Pyruvate kinase
Sulfur deficient
Sulfur-deficient
Sulphur deficient
Sulphur-deficient
Triose-phosphate isomerase deficiency

Traduction de «Carnitine deficiency » (Anglais → Français) :



Carnitine palmitoyltransferase II deficiency

déficit en carnitine palmitoyltransférase II


Adrenoleukodystrophy [Addison-Schilder] Muscle carnitine palmityltransferase deficiency

Adrénoleucodystrophie [Addison-Schilder] Carence en carnitine palmityltransférase musculaire




Andersen's disease [ Andersen disease | Najjar-Andersen syndrome | glycogenosis IV | glycogen storage disease type IV | GSD IV | alpha 1,4-glucan-6-glucosyl transferase deficiency | amylopectinosis brancher deficiency | brancher enzyme deficiency | brancher deficiency | amylopectinosis | familia ]

maladie d'Andersen [ glycogénose musculaire type IV ]


sulphur deficient [ sulphur-deficient | sulfur-deficient | sulfur deficient ]

déficient en soufre


Melanocortin 4 receptor (MC4R) deficiency is the commonest form of monogenic obesity identified so far. MC4R deficiency is characterized by severe obesity, an increase in lean body mass and bone mineral density, increased linear growth in early child

obésité par déficit du récepteur de la mélanocortine 4


Anaemia:haemolytic nonspherocytic (hereditary), type II | hexokinase deficiency | pyruvate kinase [PK] deficiency | triose-phosphate isomerase deficiency

Anémie (due à):déficit en:hexokinase | pyruvate kinase [PK] | triose-phosphate isomérase | hémolytique non sphérocytaire (héréditaire), type II




Vitamin B12 deficiency anaemia due to intrinsic factor deficiency

Anémie par carence en vitamine B12 due à une carence en facteur intrinsèque


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