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]

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

déficit congénital en lactase

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Disaccharide intolerance II

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https://browser.ihtsdotools.or (...) [HTML] [2018-01-01]

déficit congénital en héparane sulfate de l'entérocyte

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Disease that is characterized by massive enteric protein loss, secretory diarrhea and intolerance to enteral feeds during the first few weeks of life. It has been described in three male infants. Histochemical studies revealed a complete absence of e

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https://browser.ihtsdotools.or (...) [HTML] [2018-01-01]

Déficit congénital en lactase

https://icd.who.int/browse10/2 (...) (...) [HTML] [2018-01-01]

Congenital lactase deficiency

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https://icd.who.int/browse10/2 (...) [HTML] [2018-01-01]

Déficit congénital en NADH-méthémoglobine-réductase Hémoglobinose M [Hb-M] Méthémoglobinémie héréditaire

https://icd.who.int/browse10/2 (...) (...) [HTML] [2018-01-01]

Congenital NADH-methaemoglobin reductase deficiency Haemoglobin-M [Hb-M] disease Methaemoglobinaemia, hereditary

https://icd.who.int/browse10/2 (...) (...) [HTML] [2018-01-01]

https://icd.who.int/browse10/2 (...) [HTML] [2018-01-01]