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Aspartylglucosaminurie Fucosidose Mannosidose Sialidose
GM1
GM3
Gangliosidose SAI
Maladie à inclusion cellulaire
Mucolipidose
Mucolipidose I
Mucolipidose II
Mucolipidose III
Mucolipidose IV
Mucolipidose de type II
Mucolipidose type IV
Polydystrophie de type Hurler

Traduction de «mucolipidose » (Français → Anglais) :

mucolipidose de type II | mucolipidose II

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


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

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




mucolipidose type IV

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


Aspartylglucosaminurie Fucosidose Mannosidose Sialidose [mucolipidose I]

Aspartylglucosaminuria Fucosidosis Mannosidosis Sialidosis [mucolipidosis I]


Gangliosidose:SAI | GM1 | GM3 | Mucolipidose IV

Gangliosidosis:NOS | GM1 | GM3 | Mucolipidosis IV




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mucolipidose ->

Date index: 2021-10-26
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