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

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

WORLD HEALTH ORGANIZATION ICD-10: D55.2

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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

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obésité par déficit du récepteur de la mélanocortine 4

SNOMEDCT-BE (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 / 717269008

SNOMEDCT-BE (disorder) / 717269008

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Short stature due to primary acid-labile subunit (ALS) deficiency is characterized by moderate postnatal growth deficit, markedly low circulating levels of insulin-like growth factor 1 (IGF-1) and insulin-like growth factor binding protein 3 (IGFBP-3

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petite taille par déficit primaire en sous-unité acide labile

SNOMEDCT-BE (ALS) deficiency is characterized by moderate postnatal growth deficit, markedly low circulating levels of insulin-like growth factor 1 (IGF-1) and insulin-like growth factor binding protein 3 (IGFBP-3 / 721074002

SNOMEDCT-BE (disorder) / 721074002

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CLBP (ClpB homolog, mitochondrial AAA ATPase chaperonin) deficiency

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acidurie 3-méthylglutaconique type 7

SNOMEDCT-BE (ClpB homolog, mitochondrial AAA ATPase chaperonin) deficiency / 764860006

SNOMEDCT-BE (disorder) / 764860006

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Congenital multiple pituitary hormone deficiency including somatotroph, thyrotroph, lactotroph, corticotroph or gonadotroph deficiencies, due to mutations of pituitary transcription factors involved in pituitary ontogenesis. Rare when compared with t

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déficits hypohysaires multiples de cause génétique identifée

SNOMEDCT-BE (disorder) / 718182008

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Disease that is characterized clinically by neonatal hyperpigmentation, hypoglycemia, failure to thrive, and recurrent infections and biochemically by glucocorticoid deficiency without mineralocorticoid deficiency. The disease usually presents in inf

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déficit isolé familial en glucocorticoïdes

SNOMEDCT-BE (disorder) / 765326001

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endemic conditions associated with environmental iodine deficiency either directly or as a consequence of maternal iodine deficiency. Some of the conditions have no current hypothyroidism but are the consequence of inadequate thyroid hormone secretion in the developing fetus. Environmental goitrogens may be associated.

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maladies endémiques dues à une insuffisance en iode de l'environnement soit directe, soit résultant d'une insuffisance thyroïdienne maternelle. Certaines de ces maladies ne correspondent pas à une hypothyroïdie en cours mais sont la conséquence d'une sécrétion anormale de l'hormone thyroïdienne au cours du développement du fœtus. Le goitre endémique peut y être associé.

WORLD HEALTH ORGANIZATION ICD-10: E00

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Deficiency of coagulation factor due to:liver disease | vitamin K deficiency

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Carence en facteur de coagulation due à:affections du foie | avitaminose K

WORLD HEALTH ORGANIZATION ICD-10: D68.4

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WORLD HEALTH ORGANIZATION ICD-10: D68.2

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Vitamin B12 deficiency anaemia due to intrinsic factor deficiency

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

WORLD HEALTH ORGANIZATION ICD-10: D51.0

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Others have searched : congenital afibrinogenaemia deficiency ac globulin deficiency of factor hageman stuart-prower deficiency fibrin-stabilizing fibrinogen hexokinase deficiency labile proaccelerin prothrombin pyruvate kinase stable triose-phosphate isomerase deficiency vitamin k deficiency Hexokinase deficiency

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'Hexokinase deficiency'

Date index:2022-07-10 -

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Translation of "Hexokinase deficiency " (English → French) :

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