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Bessel-Hagen disease
Cerebral lipidosis
Dementia in cerebral lipidosis
Diagnosis and management of hereditary disorders
Epilepsy
Hepatolenticular degeneration
Hereditary deforming chondrodysplasia
Hereditary disposition
Hereditary lipidosis
Hereditary multiple exostosis
Hereditary predisposition
Hypercalcaemia
Intoxications
Medical genetics
Multiple cartilaginous exostoses
Multiple exostosis
Multiple osteochondromas
Multiple sclerosis
Neurosyphilis
Niacin deficiency
Pellagra
Polyarteritis nodosa
Sulfatide lipidosis
Systemic lupus erythematosus
Vitamin B12 deficiency

Traduction de «hereditary lipidosis » (Anglais → Néerlandais) :

hereditary lipidosis
http://iate.europa.eu/FindTerm (...) (...) [HTML] [2017-12-31]
erfelijke dyslipoïdose
http://iate.europa.eu/FindTerm (...) (...) [HTML] [2017-12-31]
http://iate.europa.eu/FindTerm (...) [HTML] [2017-12-31]
Bessel-Hagen disease | hereditary deforming chondrodysplasia | hereditary multiple exostosis | multiple cartilaginous exostoses | multiple exostosis | multiple osteochondromas
http://iate.europa.eu/FindTerm (...) (...) [HTML] [2017-12-31]
heriditaire multiple exostose | multiple erfelijk osteochondroom | HME [Abbr.]
http://iate.europa.eu/FindTerm (...) (...) [HTML] [2017-12-31]
http://iate.europa.eu/FindTerm (...) [HTML] [2017-12-31]
hereditary disposition | hereditary predisposition
http://iate.europa.eu/FindTerm (...) (...) [HTML] [2017-12-31]
erfelijke aanleg
http://iate.europa.eu/FindTerm (...) (...) [HTML] [2017-12-31]
http://iate.europa.eu/FindTerm (...) [HTML] [2017-12-31]
Cerebral lipidosis
https://browser.ihtsdotools.or (...) (...) [HTML] [2018-01-01]
cerebrale lipidose
https://browser.ihtsdotools.or (...) (...) [HTML] [2018-01-01]
https://browser.ihtsdotools.or (...) [HTML] [2018-01-01]
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
https://browser.ihtsdotools.or (...) (...) [HTML] [2018-01-01]
erfelijke plaatsspecifieke eierstokkanker-syndroom
https://browser.ihtsdotools.or (...) (...) [HTML] [2018-01-01]
https://browser.ihtsdotools.or (...) [HTML] [2018-01-01]
Sulfatide lipidosis
https://browser.ihtsdotools.or (...) (...) [HTML] [2018-01-01]
metachromatische leukodystrofie
https://browser.ihtsdotools.or (...) (...) [HTML] [2018-01-01]
https://browser.ihtsdotools.or (...) [HTML] [2018-01-01]
Dementia in:cerebral lipidosis (E75.-+) | epilepsy (G40.-+) | hepatolenticular degeneration (E83.0+) | hypercalcaemia (E83.5+) | hypothyroidism, acquired (E01.-+, E03.-+) | intoxications (T36-T65+) | multiple sclerosis (G35+) | neurosyphilis (A52.1+) | niacin deficiency [pellagra] (E52+) | polyarteritis nodosa (M30.0+) | systemic lupus erythematosus (M32.-+) | trypanosomiasis (B56.-+, B57.-+) | vitamin B12 deficiency (E53.8+)
https://icd.who.int/browse10/2 (...) (...) [HTML] [2018-01-01]
dementie bij | epilepsie (G40.-) | dementie bij | hepatolenticulaire degeneratie (E83.0) | dementie bij | hersenlipidose (E75.-) | dementie bij | hypercalciëmie (E83.5) | dementie bij | hypothyroïdie, verworven (E01.-, E03.-) | dementie bij | intoxicaties (T36-T65) | dementie bij | lupus erythematodes disseminatus (M32.-) | dementie bij | multipele sclerose (G35) | dementie bij | neurosyfilis (A52.1) | dementie bij | niacinedeficiëntie [pellagra] (E52) | dementie bij | polyarteriitis nodosa (M30.0) | dementie bij | trypanosomiasis (B56.-, B57.-) | dementie bij | uremie (N18.5) | dementie bij | vitamine B12-deficiëntie (E53.8)
https://icd.who.int/browse10/2 (...) (...) [HTML] [2018-01-01]
https://terminologie.nictiz.nl (...) [HTML] [2018-01-01]
diagnosis and management of hereditary disorders | medical genetics
https://ec.europa.eu/esco/port (...) (...) [HTML] [2017-12-31]
medische genetica
https://ec.europa.eu/esco/port (...) (...) [HTML] [2017-12-31]
https://ec.europa.eu/esco/port (...) [HTML] [2017-12-31]
Imerslund(-Gräsbeck) syndrome Megaloblastic hereditary anaemia
https://icd.who.int/browse10/2 (...) (...) [HTML] [2018-01-01]
megaloblastaire hereditaire-anemie | syndroom van Imerslund(-Gräsbeck)
https://icd.who.int/browse10/2 (...) (...) [HTML] [2018-01-01]
https://terminologie.nictiz.nl (...) [HTML] [2018-01-01]
Adenomatosis of colon Large intestine NOS Polyposis (hereditary) of colon
https://icd.who.int/browse10/2 (...) (...) [HTML] [2018-01-01]
adenomatose van colon | dikke darm NNO | polypose (hereditair) van colon
https://icd.who.int/browse10/2 (...) (...) [HTML] [2018-01-01]
https://terminologie.nictiz.nl (...) [HTML] [2018-01-01]


D'autres ont cherché : bessel-hagen disease     cerebral lipidosis     imerslund syndrome megaloblastic hereditary anaemia     sulfatide lipidosis     epilepsy     hepatolenticular degeneration     hereditary deforming chondrodysplasia     hereditary disposition     hereditary lipidosis     hereditary multiple exostosis     hereditary predisposition     hypercalcaemia     intoxications     medical genetics     multiple cartilaginous exostoses     multiple exostosis     multiple osteochondromas     multiple sclerosis     neurosyphilis     niacin deficiency     pellagra     polyarteritis nodosa     systemic lupus erythematosus     trypanosomiasis     vitamin b12 deficiency     


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Date index: 2022-12-30
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