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Acute intermittent
Bessel-Hagen disease
Coproporphyria
Diagnosis and management of hereditary disorders
HCP
Hereditary coproporphyria
Hereditary coproporphyria Porphyria NOS
Hereditary deforming chondrodysplasia
Hereditary disposition
Hereditary multiple exostosis
Hereditary predisposition
Medical genetics
Multiple cartilaginous exostoses
Multiple exostosis
Multiple osteochondromas

Vertaling van "Hereditary coproporphyria " (Engels → Nederlands) :

hereditary coproporphyria | HCP [Abbr.]

HCP | heriditaire coproporfyrie


Hereditary coproporphyria Porphyria:NOS | acute intermittent (hepatic)

hereditaire coproporfyrie | porfyrie | NNO | porfyrie | acuut intermitterend (hepatisch)


Bessel-Hagen disease | hereditary deforming chondrodysplasia | hereditary multiple exostosis | multiple cartilaginous exostoses | multiple exostosis | multiple osteochondromas

heriditaire multiple exostose | multiple erfelijk osteochondroom | HME [Abbr.]


hereditary disposition | hereditary predisposition

erfelijke aanleg




Ovarian cancer caused by germline mutations in various genes, usually associated with additional cancer risks. The most common are breast and ovarian cancer syndrome (HBOC) due to mutations in BRCA1 and BRCA2 genes and hereditary nonpolyposis colorec

erfelijke plaatsspecifieke eierstokkanker-syndroom


diagnosis and management of hereditary disorders | medical genetics

medische genetica


Adenomatosis of colon Large intestine NOS Polyposis (hereditary) of colon

adenomatose van colon | dikke darm NNO | polypose (hereditair) van colon


Imerslund(-Gräsbeck) syndrome Megaloblastic hereditary anaemia

megaloblastaire hereditaire-anemie | syndroom van Imerslund(-Gräsbeck)


A very rare hereditary skin disease with manifestation of irregularly distributed epidermal hyperkeratosis of the palms and soles. Reported in 35 families worldwide to date. The lesions usually start to develop in early adolescence but can also prese

syndroom van Buschke-Fischer-Brauer


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