autosomaal dominante hereditaire aandoening	congenitale clinodactylie van digitus V van hand	congenitale keratosis palmoplantaris	genodermatose	hereditaire diffuse keratosis palmoplantaris	hereditaire ontwikkelingsstoornis
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syndroom van palmoplantaire keratodermie en clinodactylie (aandoening)
	syndroom van palmoplantaire keratodermie en clinodactylie
	Palmoplantar keratoderma with clinodactyly syndrome
	Keratosis palmaris et plantaris with clinodactyly syndrome
	Syndrome with the association of palmoplantar keratosis and clinodactyly of the fifth finger. Less than 20 cases have been described in the literature so far, and the majority of reported patients were of Mexican origin. Transmission is autosomal dominant.

Id	724224007
Status	Primitive

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

Associated morphology	congenitale afwijkende kromming
Finding site	structuur van digitus V van hand
Occurrence	congenitaal
Pathological process	proces van pathologische ontwikkeling

Associated morphology	hyperkeratose
Finding site	gehele huid van plantaire zijde van voet

Associated morphology	hyperkeratose
Finding site	gehele huid van palmaire zijde van hand

DHD Diagnosis thesaurus reference set

RIVM authorized national diagnosis thesaurus to ICD10 complex mapping reference set

Target	Q82.8
Term	Overige gespecificeerde congenitale misvormingen van huid

Target	Q68.1
Term	Congenitale misvorming van hand

SNOMED CT to Orphanet simple map

86919

SNOMED CT to ICD-10 extended map

Target	Q82.8
Rule	TRUE
Advice	ALWAYS Q82.8
Correlation	SNOMED CT source code to target map code correlation not specified

Target	Q68.1
Rule	TRUE
Advice	ALWAYS Q68.1
Correlation	SNOMED CT source code to target map code correlation not specified