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

Translation of "omodysplasie autosomique dominante " (French → English) :

omodysplasie autosomique dominante

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


omodysplasie autosomique récessive

Autosomal recessive omodysplasia
SNOMEDCT-BE (disorder) / 725166005
SNOMEDCT-BE (disorder) / 725166005


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


leucodystrophie autosomique dominante de l'adulte

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


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


syndrome d'atrophie optique-cataracte autosomique dominante

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


dystonie dopa-sensible autosomique dominante

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


myoglobinurie autosomique dominante

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


hypocalcémie autosomique dominante

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




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omodysplasie autosomique dominante

Date index:2023-01-21 -

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