A rare developmental defect during embryogenesis syndrome, with characteristics of normal female karyotype, normal ovaries, male or ambiguous genitalia, urinary tract malformations (ranging from bilateral renal agenesis to mild unilateral hydronephro

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syndrome d'anomalie du développement sexuel 46,XX-anomalies anorectales

SNOMEDCT-BE (ranging from bilateral renal agenesis to mild unilateral hydronephro / 733622000

SNOMEDCT-BE (disorder) / 733622000

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Agenesis of nerve Displacement of brachial plexus Jaw-winking syndrome Marcus Gunn's syndrome

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Agénésie d'un nerf Anomalie d'un plexus nerveux Mâchoire à clignement Phénomène de Marcus Gunn

WORLD HEALTH ORGANIZATION ICD-10: Q07.8

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Disease with characteristics of progressive ataxia beginning during infancy, a pyramidal syndrome and dental agenesis. The syndrome has been described in four children born to consanguineous parents. The mode of transmission is autosomal recessive.

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odontoleucodystrophie

SNOMEDCT-BE (disorder) / 722064003

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Others have searched : aicardi syndrome ivemark's syndrome potter's syndrome xy gonadal agenesis syndrome agenesis of the corpus callosum asplenia syndrome dysplasia renal facialis renal agenesis syndrome renofacial syndrome splenic agenesis syndrome splenic deficiency syndrome

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'splenic agenesis syndrome'

Date index:2024-03-20 -

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Translation of "splenic agenesis syndrome " (English → French) :

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