autosomaal recessieve hereditaire aandoening	ectodermale dysplasie met afwijking van zweetklieren	hereditaire aandoening van integumentum	hereditaire ontwikkelingsstoornis
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syndroom van hypohidrotische ectodermale dysplasie, hypothyreoïdie en ciliaire dyskinesie (aandoening)
	syndroom van hypohidrotische ectodermale dysplasie, hypothyreoïdie en ciliaire dyskinesie
	hypohidrotische ectodermale dysplasie-hypothyroïdie-ciliaire dyskinesie-syndroom ANOTHER-syndroom HEDH-syndroom
	Alopecia, nail dystrophy, ophthalmic complications, thyroid dysfunction, hypohidrosis, ephelides, enteropathy and respiratory tract infections
	Hypohidrotic ectodermal dysplasia, hypothyroidism, ciliary dyskinesia syndrome ANOTHER (alopecia, nail dystrophy, ophthalmic complications, thyroid dysfunction, hypohidrosis, ephelides, enteropathy, respiratory tract infection) syndrome ANOTHER syndrome

Id	239050000
Status	Primitive

Associated morphology	dysplasie
Finding site	structuur van ectoderm
Occurrence	congenitaal
Pathological process	proces van pathologische ontwikkeling

Associated morphology	morfologische afwijking
Finding site	structuur van huid
Occurrence	congenitaal
Pathological process	proces van pathologische ontwikkeling

Has interpretation	afwijkend
Interprets	zweten

SNOMED CT to Orphanet simple map

RIVM authorized national diagnosis thesaurus to ICD10 complex mapping reference set

Target	Q84.0
Term	Congenitale alopecia

SNOMED CT to ICD-10 extended map

Target	Q84.0
Rule	TRUE
Advice	ALWAYS Q84.0
Correlation	SNOMED CT source code to target map code correlation not specified