Disease that is characterized clinically by neonatal hyperpigmentation, hypoglycemia, failure to thrive, and recurrent infections and biochemically by glucocorticoid deficiency without mineralocorticoid deficiency. The disease usually presents in inf

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déficit isolé familial en glucocorticoïdes

SNOMEDCT-BE (disorder) / 765326001

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biochemical evidence of deficiency

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signe biochimique de carence

IATE - Health

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Others have searched : auxotroph biochemical evidence of deficiency biochemical mutant biochemically deficient mutant

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'biochemically deficient mutant'

Date index:2023-10-07 -

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Translation of "biochemically deficient mutant " (English → French) :

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