aandoening van bovenste deel van tractus gastrointestinalis	autosomaal dominante hereditaire aandoening	genetische aandoening van huidpigmentatie	hereditaire aandoening van integumentum	hereditaire aandoening van spijsverteringsstelsel	hyperpigmentatie
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gastrocutaan syndroom (aandoening)
	gastrocutaan syndroom
	Gastrocutaneous syndrome
	A rare, syndromic, hyperpigmentation of the skin characterized by multiple lentigines and café-au-lait spots associated with hiatal hernia and peptic ulcer, hypertelorism and myopia. There have been no further descriptions in the literature since 1982.

Id	782946000
Status	Primitive

Associated morphology	hyperpigmentatie
Finding site	structuur van huid

Finding site

structuur van bovenste deel van tractus gastrointestinalis

SNOMED CT to Orphanet simple map

RIVM authorized national diagnosis thesaurus to ICD10 complex mapping reference set

Target	L81.8
Term	Overige gespecificeerde pigmentatiestoornissen

Target	K92.8
Term	Overige gespecificeerde ziekten van spijsverteringsstelsel

SNOMED CT to ICD-10 extended map

Target	Q85.8
Rule	TRUE
Advice	ALWAYS Q85.8 \| POSSIBLE REQUIREMENT FOR ADDITIONAL CODE TO FULLY DESCRIBE DISEASE OR CONDITION
Correlation	SNOMED CT source code to target map code correlation not specified