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Constitutional
Growth hormone
Insufficiency NOS
Laron-type
Nutritional short stature
Physical retardation due to malnutrition
Pituitary hormone
Psychosocial
Sheehan's syndrome Simmonds' disease
Short stature
Short stature NOS
Stunting

Vertaling van "nutritional short stature " (Engels → Nederlands) :

Nutritional:short stature | stunting | Physical retardation due to malnutrition

groeiretardatiedoor ondervoeding | korte gestaltedoor ondervoeding | lichamelijke achterstanddoor ondervoeding


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

dwerggroei van Lorain-Levi | fertiel eunuchoïdisme | geïsoleerde deficiëntie van | ACTH | geïsoleerde deficiëntie van | gonadotropine | geïsoleerde deficiëntie van | groeihormoon | geïsoleerde deficiëntie van | hypofysair hormoon | hypofysaire | cachexie | hypofysaire | insufficiëntie NNO | hypofysaire | kleine gestalte | hypogonadotroop hypogonadisme | idiopathische groeihormoondeficiëntie | necrose van hypofyse (post partum) | panhypopituïtarisme | syndroom van Kallmann | syndroom van Sheehan | ziekte van Simmonds


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

syndroom van Fenton-Wilkinson-Toselano


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

X-gebonden colobomateuze microftalmie, microcefalie, intellectuele achterstand, kleine gestalte-syndroom


An extremely rare partial autosomal tetrasomy, resulting from a partial triplication of the long arm of chromosome 11, with characteristics of intellectual disability (with severe verbal impairment), short stature with small extremities, keratoconus

tetrasomie 11q24.1


Short stature:NOS | constitutional | Laron-type | psychosocial

kleine gestalte: | NNO | kleine gestalte: | constitutioneel | kleine gestalte: | Laron-type | kleine gestalte: | psychosociaal




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Date index: 2023-03-24
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