aandoening van niet-coronaire systemische arterie	afwijking van bloedvat van onderste extremiteit	autosomaal recessieve hereditaire aandoening	calcificatie van gewricht	hereditaire aandoening van bewegingsapparaat	hereditaire aandoening van cardiovasculair systeem	vasculaire calcificatie
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hereditair syndroom van arteriële en articulaire meervoudige calcificaties (aandoening)
	hereditair syndroom van arteriële en articulaire meervoudige calcificaties
	syndroom van hereditaire arteriële en articulaire multipele calcificaties
	Hereditary arterial and articular multiple calcification syndrome
	A very rare genetic vascular disease of autosomal recessive inheritance, described in less than 20 patients to date. The disease has manifestations of adult-onset (as early as the second decade of life) isolated calcification of the arteries of the lower extremities (including the iliac, femoral, and tibial arteries) as well as the capsule joints of the fingers, wrists, ankles and feet.

Id	718602007
Status	Primitive

Associated morphology	pathologische calcificatie
Finding site	structuur van gewricht

Associated morphology	pathologische calcificatie
Finding site	structuur van arterie van onderste extremiteit

DHD Diagnosis thesaurus reference set

RIVM authorized national diagnosis thesaurus to ICD10 complex mapping reference set

Target	I70.20
Term	Atherosclerose van arteriën van extremiteiten zonder gangreen

Target	M25.80
Term	Overige gespecificeerde gewrichtsaandoeningen van multipele lokalisaties

SNOMED CT to Orphanet simple map

289601

SNOMED CT to ICD-10 extended map

Target	I70.20
Rule	TRUE
Advice	ALWAYS I70.20 \| POSSIBLE REQUIREMENT FOR ADDITIONAL CODE TO FULLY DESCRIBE DISEASE OR CONDITION
Correlation	SNOMED CT source code to target map code correlation not specified

Target	M25.80
Rule	TRUE
Advice	ALWAYS M25.80
Correlation	SNOMED CT source code to target map code correlation not specified