autosomaal dominante hereditaire aandoening	dystrophia unguium	erytrokeratodermie	genetische nagelaandoening	hereditaire aandoening van auditief systeem	hypotrichosis	perceptief gehoorverlies
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syndroom van hypotrichose en doofheid (aandoening)
	syndroom van hypotrichose en doofheid
	Hypotrichosis and deafness syndrome
	A syndromic genetic deafness with characteristics of erythrokeratoderma, hypotrichosis, nail dystrophy and sensorineural hearing loss. Erythema, recurrent skin infections and mucositis have also been associated.

Id	783555001
Status	Primitive

Associated morphology	dystrofie
Finding site	structuur van nagel

Associated morphology	verandering in groei
Finding site	structuur van pilus

Finding site

structuur van auditief systeem

Has interpretation	afwijkend
Interprets	keratinisatie

Interprets

DHD Diagnosis thesaurus reference set

RIVM authorized national diagnosis thesaurus to ICD10 complex mapping reference set

Target	H90.5
Term	Gehoorverlies door perceptiestoornis, niet gespecificeerd

SNOMED CT to Orphanet simple map

330029

SNOMED CT to ICD-10 extended map

Target	H90.5
Rule	TRUE
Advice	ALWAYS H90.5 \| POSSIBLE REQUIREMENT FOR ADDITIONAL CODE TO FULLY DESCRIBE DISEASE OR CONDITION
Correlation	SNOMED CT source code to target map code correlation not specified