aandoening van adenohypofyse	autosomaal dominante hereditaire aandoening	hereditaire aandoening van endocrien systeem	hereditaire aandoening van immuunsysteem	hereditaire aandoening van zenuwstelsel	hypopituïtarisme	primaire immunodeficiëntie
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syndroom van disfunctie van adenohypofyse en 'common variable immunodeficiency' (aandoening)
	syndroom van disfunctie van adenohypofyse en 'common variable immunodeficiency'
	syndroom van adenohypofysaire disfunctie en CVID
	Deficiency in anterior pituitary function, variable immunodeficiency syndrome
	DAVID (deficiency in anterior pituitary function, variable immunodeficiency) syndrome
	A rare, genetic endocrine disease characterized by the association of common variable immunodeficiency, manifesting with hypogammaglobulinemia and recurrent or severe childhood-onset sinopulmonary infections, followed, possibly many years later, by symptomatic adrenocorticotropic hormone (ACTH) deficiency resulting from anterior pituitary hormone deficiency.

Id	773664005
Status	Primitive

Finding site

structuur van adenohypofyse

Pathological process

afwijkend immuunproces

DHD Diagnosis thesaurus reference set

RIVM authorized national diagnosis thesaurus to ICD10 complex mapping reference set

Target	E23.0
Term	Hypopituïtarisme

Target	D89.8
Term	Overige gespecificeerde aandoeningen waarbij immuunsysteem betrokken is, niet elders geclassificeerd

SNOMED CT to Orphanet simple map

293978

SNOMED CT to ICD-10 extended map

Target	E23.0
Rule	TRUE
Advice	ALWAYS E23.0 \| POSSIBLE REQUIREMENT FOR ADDITIONAL CODE TO FULLY DESCRIBE DISEASE OR CONDITION
Correlation	SNOMED CT source code to target map code correlation not specified

Target	D83.8
Rule	TRUE
Advice	ALWAYS D83.8
Correlation	SNOMED CT source code to target map code correlation not specified