Vertaling van "polypeptide hormone " (Engels → Nederlands) :

polypeptide hormone
polypeptidehormoon

Increased secretion from endocrine pancreas of:growth hormone-releasing hormone | pancreatic polypeptide | somatostatin | vasoactive-intestinal polypeptide
verhoogde secretie vanuit endocriene pancreas van | groeihormoon-releasing hormoon [GH-RH] | verhoogde secretie vanuit endocriene pancreas van | pancreaspolypeptide [PP] | verhoogde secretie vanuit endocriene pancreas van | somatostatine | verhoogde secretie vanuit endocriene pancreas van | vasoactive-intestinal polypeptide [VIP]

Describes a rare group of immunodeficiencies due to specific mutations in the inhibitor of kappa light polypeptide gene enhancer in B-cells, kinase gamma (IKBKG) or the cytochrome b-245, beta polypeptide (CYBB) genes. The clinical manifestation is my
X-gebonden Mendeliaanse gevoeligheid voor mycobacteriële ziekten

hormonal substance | substance having a hormonal action | substance with hormonal action
stof met hormonale werking

growth hormone | human growth hormone | somatotropic hormone | HGH [Abbr.] | STH [Abbr.]
hGH | humaan groeihormoon | menselijk groeihormoon | somatotropine

A type of central congenital hypothyroidism with characteristics of low levels of thyroid hormones due to insufficient release of thyroid-stimulating hormone (TSH) caused by pituitary resistance to thyrotropin-releasing hormone (TRH). It may or may n
congenitale centrale hypothyreoïdie door deficiëntie van thyrotropine-'releasing'-hormoonreceptor

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

polypeptide | amino acid polymer
polypeptide | keten van een groot aantal met elkaar verbonden aminozuren

Primary pigmented nodular adrenocortical disease (PPNAD) is a form of bilateral adrenocortical hyperplasia that is often associated with adrenocorticotrophin hormone independent Cushing syndrome. The disease has characteristics of small to normal siz
primaire gepigmenteerde nodulaire adrenocorticale ziekte

Autosomal recessive agammaglobulinaemia (Swiss type) X-linked agammaglobulinaemia [Bruton] (with growth hormone deficiency)
autosomale recessieve-agammaglobulinemie (Swiss type) | X-gebonden agammaglobulinemie [Bruton] (met groeihormoondeficiëntie)