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Adermatoglyphie congénitale isolée
Anorchidie congénitale isolée
Mégalocornée isolée congénitale
Paralysie faciale congénitale héréditaire isolée

Translation of "Anorchidie congénitale isolée " (French → English) :

anorchidie congénitale isolée

XY Gonadal agenesis syndrome
SNOMEDCT-BE (disorder) / 53599007
SNOMEDCT-BE (disorder) / 53599007


adermatoglyphie congénitale isolée

A rare genetic developmental defect during embryogenesis disorder with characteristics of the lack of epidermal ridges on the palms and soles, resulting in the absence of fingerprints, with no other associated manifestations. It is associated with a
SNOMEDCT-BE (disorder) / 763748007
SNOMEDCT-BE (disorder) / 763748007


paralysie faciale congénitale héréditaire isolée

An extremely rare neurological disorder presumed to result from maldevelopment of the facial nucleus and/or cranial nerve reported in fewer than 10 families to date. It manifests as non-progressive, isolated, unilateral or bilateral, symmetrical or a
SNOMEDCT-BE (disorder) / 733091002
SNOMEDCT-BE (disorder) / 733091002


mégalocornée isolée congénitale

Isolated congenital megalocornea is a genetic, non-syndromic developmental defect of the anterior eye segment. The disease has characteristics of bilateral enlargement of the corneal diameter and a deep anterior eye chamber, without an elevation in i
SNOMEDCT-BE (disorder) / 734026006
SNOMEDCT-BE (disorder) / 734026006




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Anorchidie congénitale isolée

Date index:2021-11-06 -

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