A rare genetic immuno-osseous dysplasia disorder with characteristics of pre and post-natal growth retardation, hypotonia, borderline to moderate intellectual disability, retinal dystrophy, spondyloepiphyseal dysplasia (epiphyseal dysplasia, epiphyse

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syndrome de Roifman

SNOMEDCT-BE (epiphyseal dysplasia, epiphyse / 773404000

SNOMEDCT-BE (disorder) / 773404000

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Canadian Society for Ectodermal Dysplasias

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Canadian Society for Ectodermal Dysplasias

National Bodies and Committees (Canadian) | The Skin

Organismes et comités nationaux canadiens | Appareil cutané

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Omodysplasia is a rare skeletal dysplasia characterised by severe limb shortening and facial dysmorphism. Two types of omodysplasia have been described: an autosomal recessive or generalised form (also referred to as micromelic dysplasia with disloca

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omodysplasie

SNOMEDCT-BE / 725164008

SNOMEDCT-BE (disorder) / 725164008

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Multiple epiphyseal dysplasia with severe proximal femoral dysplasia

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dysplasie épiphysaire multiple avec dysplasie fémorale sévère

SNOMEDCT-BE (disorder) / 763893008

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Others have searched : canadian society for ectodermal dysplasias christ-siemens syndrome ellis-van creveld syndrome d multiple epiphyseal dysplasia pyle's disease siemens'syndrome anhidrotic ectodermal dysplasia chondroectodermal dysplasia congenital ectodermal dysplasia craniometaphyseal dysplasia dysplasia of hip ectodermal dysplasia hereditary ectodermal dysplasia hip dysplasia mesoectodermal dysplasia metaphyseal dysplasia

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'mesoectodermal dysplasia'

Date index:2023-12-27 -

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Translation of "mesoectodermal dysplasia " (English → French) :

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