Traduction de «mucolipidose iv » (Français → Anglais) :

Gangliosidose:SAI | GM1 | GM3 | Mucolipidose IV

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

Gangliosidosis:NOS | GM1 | GM3 | Mucolipidosis IV

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

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

mucolipidose de type II | mucolipidose II

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

I-cell disease | mucolipidosis II | ICD [Abbr.] | ML II [Abbr.]

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

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

mucolipidose

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

mucolipidosis

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

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

mucolipidose type IV

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

A lysosomal storage disease with clinical characteristics of psychomotor retardation and visual abnormalities including corneal clouding, retinal degeneration or strabismus. The disease is rare in the general population but is more prevalent among As

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

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

Mucolipidose II [maladie à inclusion cellulaire] Mucolipidose III [polydystrophie de type Hurler]

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

Mucolipidosis II [I-cell disease] Mucolipidosis III [pseudo-Hurler polydystrophy]

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

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

Aspartylglucosaminurie Fucosidose Mannosidose Sialidose [mucolipidose I]

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

Aspartylglucosaminuria Fucosidosis Mannosidosis Sialidosis [mucolipidosis I]

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

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