A heterogeneous group disorders characterized by short, brittle hair with low-sulfur content (due to an abnormal synthesis of the sulfur containing keratins). The abnormalities are usually obvious at birth, with variable clinical expression. Trichoth

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trichothiodystrophie

SNOMEDCT-BE (due to an abnormal synthesis of the sulfur containing keratins). The abnormalities are usually obvious at birth, with variable clinical expression. Trichoth / 723551003

SNOMEDCT-BE (disorder) / 723551003

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Pollutants

Agents de pollution

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G6PD deficiency | g-6-p-d deficiency | glucose 6-dehydrogenase deficiency | glucose-6-phosphate dehydrogenase deficiency

http://iate.europa.eu/FindTerm (...) (...) [HTML] [2017-12-31]

déficit en G6PD | déficit en glucose-6-phosphate-déshydrogénase

IATE - Health

http://iate.europa.eu/FindTerm (...) (...) [HTML] [2017-12-31]

http://iate.europa.eu/FindTerm (...) [HTML] [2017-12-31]

sulfur chloride | sulfur subchloride | sulfur monochloride

http://gdt.oqlf.gouv.qc.ca/fic (...) (...) [HTML] [2018-01-01]

monochlorure de soufre | chlorure de soufre

chimie > chimie minérale

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http://gdt.oqlf.gouv.qc.ca/fic (...) [HTML] [2018-01-01]

congenital antithrombin III deficiency | congenital deficiency of antithrombin III | inherited antithrombin III deficiency | inherited deficiency in AT III

http://gdt.oqlf.gouv.qc.ca/fic (...) (...) [HTML] [2018-01-01]

déficit congénital en antithrombine III

médecine > anatomopathologie | médecine > hématologie et sérologie

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http://gdt.oqlf.gouv.qc.ca/fic (...) [HTML] [2018-01-01]

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maladie d'Andersen [ glycogénose musculaire type IV ]

Endocrine System and Metabolism | Liver and Biliary Ducts

Systèmes endocrinien et métabolique | Foie et voies biliaires

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deficiency disease | nutrition deficiency disease | nutritional deficiency disease

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maladie de carence | maladie par carence alimentaire

médecine > diététique et nutrition

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http://gdt.oqlf.gouv.qc.ca/fic (...) [HTML] [2018-01-01]

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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Green sulfur bacteria

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Familia Chlorobiaceae

SNOMEDCT-BE (organism) / 414199005

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Others have searched : andersen disease andersen's disease g6pd deficiency gsd iv green sulfur bacteria najjar-andersen syndrome amylopectinosis amylopectinosis brancher deficiency bisulfite brancher deficiency brancher enzyme deficiency congenital antithrombin iii deficiency congenital deficiency of antithrombin iii deficiency disease familia g-6-p-d deficiency glucose 6-dehydrogenase deficiency glucose-6-phosphate dehydrogenase deficiency glycogen storage disease type iv glycogenosis iv inherited antithrombin iii deficiency inherited deficiency in at iii nutrition deficiency disease nutritional deficiency disease sulfur chloride sulfur deficient sulfur dioxide sulfur monochloride sulfur subchloride sulfur-deficient sulfurous acid anhydride sulfurous anhydride sulfurous oxide sulphur deficient sulphur dioxide sulphur-deficient sulphurous anhydride sulphurous oxide Sulfur deficient

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'Sulfur deficient'

Date index:2023-03-05 -

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Translation of "Sulfur deficient " (English → French) :

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