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Translation of "short stature " (English → French) :
TERMINOLOGY
see also In-Context Translations below A rare genetic multiple congenital anomalies/dysmorphic syndrome with characteristics of cerebellar-like ataxia, photosensitivity (mainly of the face and trunk), short stature and intellectual disability. Additional features include clinodactyly, sin
syndrome d'ataxie-photosensibilité-petite taille
SNOMEDCT-BE (mainly of the face and trunk), short stature and intellectual disability. Additional features include clinodactyly, sin / 773769008
SNOMEDCT-BE (disorder) / 773769008
Fertile eunuch syndrome Hypogonadotropic hypogonadism Idiopathic growth hormone deficiency Isolated deficiency of:gonadotropin | growth hormone | pituitary hormone | Kallmann's syndrome Lorain-Levi short stature Necrosis of pituitary gland (postpartum) Panhypopituitarism Pituitary:cachexia | insufficiency NOS | short stature | Sheehan's syndrome Simmonds' disease
Cachexie hypophysaire Hypogonadisme hypogonadotrophique Insuffisance (de):hormone de croissance idiopathique | isolée en:gonadotrophine | hormone de croissance | hormone hypophysaire | staturale pituitaire SAI | Maladie de Simmonds Nécrose pituitaire (post-partum) Panhypopituitarisme Syndrome de:eunuchoïdisme fertile | Kallmann | Lorain-Lévi | Sheehan
WORLD HEALTH ORGANIZATION ICD-10: E23.0
WORLD HEALTH ORGANIZATION ICD-10: E23.0
A rare syndromic microphthalmia disorder with characteristics of microphthalmia with coloboma (which may involve the iris, ciliary body, choroid, retina and/or optic nerve), microcephaly, short stature and intellectual disability. Other eye abnormali
syndrome de micropthalmie colobomateuse-microcéphalie-déficience intellectuelle-petite taille liée à l'X
SNOMEDCT-BE (which may involve the iris, ciliary body, choroid, retina and/or optic nerve), microcephaly, short stature and intellectual disability. Other eye abnormali / 771148008
SNOMEDCT-BE (disorder) / 771148008
A rare genetic syndromic intellectual disability characterised by mild intellectual disability, short stature with high body mass index, short neck with cervical gibbus and dysmorphic facial features. A metabolic syndrome, including type 2 diabetes,
del(9)(q31.1q31.3)
SNOMEDCT-BE (disorder) / 773493002
SNOMEDCT-BE (disorder) / 773493002
This syndrome has characteristics of severe short stature with disproportionately short legs, small hands, clinodactyly, valvular heart disease and dysmorphism (ptosis, high-arched palate, abnormal dentition). It has been described in a mother and tw
syndrome de petite taille-valvulopathie cardiaque-dysmorphie
SNOMEDCT-BE (ptosis, high-arched palate, abnormal dentition). It has been described in a mother and tw / 716193004
SNOMEDCT-BE (disorder) / 716193004
A rare genetic syndromic intellectual disability characterized by mild intellectual disability, short stature with high body mass index, short neck with cervical gibbus and dysmorphic facial features. A metabolic syndrome, including type 2 diabetes,
syndrome de microdélétion 9 q31.1q31.3
SNOMEDCT-BE (disorder) / 773493002
SNOMEDCT-BE (disorder) / 773493002
Syndrome with characteristics of caudal appendage, short terminal phalanges, deafness, cryptorchidism, intellectual deficit, short stature and dysmorphism. It has been described in monozygotic twin boys.
syndrome d'appendice caudal-surdité
SNOMEDCT-BE (disorder) / 726621009
SNOMEDCT-BE (disorder) / 726621009
Rare syndrome with characteristics of the combination of polyvalvular heart disease, short stature, facial anomalies and intellectual deficit. Dysplasia may involve the mitral, tricuspidal, aortic and pulmonary valves. Dysmorphic facial anomalies are
syndrome de la maladie cardiaque polyvalvulaire
SNOMEDCT-BE (disorder) / 723448007
SNOMEDCT-BE (disorder) / 723448007
A rare chromosomal anomaly syndrome with a highly variable phenotype. Principle characteristics are a neonatal mewing cry, severe developmental delay and intellectual disability, short stature, hypotonia, dysmorphic features (including microcephaly,
syndrome du chromosome 5 en anneau
SNOMEDCT-BE (including microcephaly, / 765487008
SNOMEDCT-BE (disorder) / 765487008
This syndrome has characteristics of X-linked intellectual deficit and mild variable manifestations, including short stature, small head circumference, sloping forehead, hearing loss, abnormally shaped ears, and small testes. It has been described in
déficience intellectuelle liée à l'X type Abidi
SNOMEDCT-BE (disorder) / 719018008
SNOMEDCT-BE (disorder) / 719018008
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'short stature'
Date index:2024-03-12 -
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