autosomaal recessieve hereditaire aandoening
syndroom van resistentie voor adrenocorticotroop hormoon
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familiaire deficiëntie van glucocorticoïd (aandoening)
familiaire deficiëntie van glucocorticoïd
familiale glucocorticoïddeficiëntie
Familial glucocorticoid deficiency
Familial glucocorticoid deficiency (FGD) is a group of primary adrenal insufficiencies characterized clinically by neonatal hyperpigmentation, hypoglycemia, failure to thrive, and recurrent infections, and biochemically by glucocorticoid deficiency without mineralocorticoid deficiency.
Id765326001
StatusPrimitive
Finding sitestructuur van bijnierschors
Finding sitestructuur van schildklier
Occurrencecongenitaal
DHD Diagnosis thesaurus reference set
RIVM authorized national diagnosis thesaurus to ICD10 complex mapping reference set
TargetE27.1
TermPrimaire bijnierschorsinsufficiëntie
SNOMED CT to Orphanet simple map361
SNOMED CT to ICD-10 extended map
TargetE27.1
RuleTRUE
AdviceALWAYS E27.1 | POSSIBLE REQUIREMENT FOR ADDITIONAL CODE TO FULLY DESCRIBE DISEASE OR CONDITION
CorrelationSNOMED CT source code to target map code correlation not specified