A rare mitochondrial disease due to a defect in mitochondrial protein synthesis with a variable phenotype that includes onset in infancy or early childhood of failure to thrive and psychomotor regression (after initial normal development), as well as

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déficit combiné de la phosphorylation oxydative type 7

SNOMEDCT-BE (after initial normal development), as well as / 763204003

SNOMEDCT-BE (disorder) / 763204003

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Chancre of yaws Framboesia, initial or primary Initial framboesial ulcer Mother yaw

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Chancre pianique Frambœsia initiale ou primaire Pian mère Ulcère frambœsial initial

WORLD HEALTH ORGANIZATION ICD-10: A66.0

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https://icd.who.int/browse10/2 (...) [HTML] [2018-01-01]

completing initial resource statements | initial resource statements production | complete initial resource statements | production of initial resource statements

https://ec.europa.eu/esco/port (...) (...) [HTML] [2017-12-31]

remplir des déclarations initiales de ressources

skill

Aptitude

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initiating efficiency | initiating power | initiating strength | initiating value

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pouvoir d'amorcage | puissance d'amorcage

IATE - Coal and mining industries

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http://iate.europa.eu/FindTerm (...) [HTML] [2017-12-31]

Community initiative concerning the improvement in tendering for services by businesses in Objective 1 regions | Community Initiative concerning the Preparation of Businesses for the Single Market | Community initiative concerning the preparation of businesses for the Single Market(P reparation of R egional I ndustry for the S ingle Ma rket) | PRISMA [Abbr.]

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Initiative communautaire concernant la préparation des entreprises dans la perspective du Marché Unique

IATE - ECONOMICS | European construction

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http://iate.europa.eu/FindTerm (...) [HTML] [2017-12-31]

A rare non-dystrophic myopathy with characteristics of slowly progressive muscular weakness and atrophy initially involving proximal lower limbs and hip girdle and later on shoulder girdle, proximal upper limbs and axial muscles. Ambulation is usuall

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myopathie à corps d'inclusion héréditaire type 4

SNOMEDCT-BE (disorder) / 770786001

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A disorder of the skin and immune system with initial manifestation of a bumpy skin rash usually between the ages of 6 and 12 months, gradually spreading from the arms and legs to the torso and face. At about age 2, the rash fades leaving hyperpigmen

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poïkilodermie avec neutropénie

SNOMEDCT-BE (disorder) / 772126000

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Initial stage of trachoma

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Phase initiale du trachome

WORLD HEALTH ORGANIZATION ICD-10: A71.0

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Initial lesions of yaws