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Brachyolmie autosomique dominante
Dystonie dopa-sensible autosomique dominante
Hypocalcémie autosomique dominante
Kératite autosomique dominante
Leucodystrophie autosomique dominante de l'adulte
Microcéphalie primaire autosomique dominante
Myoglobinurie autosomique dominante
Omodysplasie autosomique dominante

Translation of "Dominante " (French → English) :

TERMINOLOGY
see also In-Context Translations below
leucodystrophie autosomique dominante de l'adulte

Adult onset autosomal dominant leucodystrophy
SNOMEDCT-BE (disorder) / 448054001
SNOMEDCT-BE (disorder) / 448054001


myoglobinurie autosomique dominante

Autosomal dominant myoglobinuria
SNOMEDCT-BE (disorder) / 725903003
SNOMEDCT-BE (disorder) / 725903003


dystonie dopa-sensible autosomique dominante

Autosomal dominant Segawa syndrome
SNOMEDCT-BE (disorder) / 715768000
SNOMEDCT-BE (disorder) / 715768000


syndrome d'atrophie optique-cataracte autosomique dominante

Autosomal dominant optic atrophy type 3
SNOMEDCT-BE (disorder) / 719517009
SNOMEDCT-BE (disorder) / 719517009


omodysplasie autosomique dominante

Autosomal dominant omodysplasia
SNOMEDCT-BE (disorder) / 725165009
SNOMEDCT-BE (disorder) / 725165009


hypocalcémie autosomique dominante

Autosomal dominant hypocalcemia
SNOMEDCT-BE (disorder) / 711152006
SNOMEDCT-BE (disorder) / 711152006


amyotrophie spinale proximale autosomique dominante de l'enfance

Disease with characteristics of muscle weakness and atrophy in the lower limbs, most severely affecting the quadriceps. The loss of motor neurons leads to atrophy of the muscles in the lower limbs with manifestations including unsteady walk and walki
SNOMEDCT-BE (disorder) / 772129007
SNOMEDCT-BE (disorder) / 772129007


kératite autosomique dominante

Autosomal dominant keratitis
SNOMEDCT-BE (disorder) / 715339004
SNOMEDCT-BE (disorder) / 715339004


brachyolmie autosomique dominante

Autosomal dominant brachyolmia
SNOMEDCT-BE (disorder) / 717264003
SNOMEDCT-BE (disorder) / 717264003


microcéphalie primaire autosomique dominante

Autosomal dominant primary microcephaly
SNOMEDCT-BE (disorder) / 778070003
SNOMEDCT-BE (disorder) / 778070003
IN-CONTEXT TRANSLATIONS


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Dominante

Date index:2021-12-16 -

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