Autosomal dominant hereditary disorder	Congenital anomaly of oral mucosa	Congenital anomaly of skin	Congenital dysplasia	Developmental hereditary disorder	Digestive system hereditary disorder	Dyskeratosis	Hereditary disorder of the integument	Lesion of oral mucosa	Skin lesion
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Hereditary benign intraepithelial dyskeratosis (disorder)
	Hereditary benign intraepithelial dyskeratosis
	Witkop-von Sallman syndrome Witkop-Von Sallmann disease
	hereditaire benigne intra-epitheliale dyskeratose
	erfelijke benigne corneale intra-epitheliale dyskeratose HBID syndroom van Witkop-von Sallman

Id	400014002
Status	Primitive

Associated morphology	Dyskeratosis
Finding site	Skin structure
Occurrence	Congenital
Pathological process	Pathological developmental process

Associated morphology	Dyskeratosis
Finding site	Oral mucous membrane structure
Occurrence	Congenital
Pathological process	Pathological developmental process

DHD Diagnosis thesaurus reference set

ICD-10 complex map reference set

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