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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.
Id718602007
StatusPrimitive
Associated morphologypathologische calcificatie
Finding sitestructuur van gewricht
referentieset met complexe 'mapping' naar ICD-10
TargetI70.20
RuleTRUE
AdviceALWAYS I70.20 | POSSIBLE REQUIREMENT FOR ADDITIONAL CODE TO FULLY DESCRIBE DISEASE OR CONDITION
CorrelationSNOMED CT source code to target map code correlation not specified
TargetM25.80
RuleTRUE
AdviceALWAYS M25.80
CorrelationSNOMED CT source code to target map code correlation not specified