autosomaal recessieve hereditaire aandoening	hereditaire aandoening van bewegingsapparaat	hereditaire ontwikkelingsstoornis	lengtedefect van metacarpus	osteolyse
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syndroom van osteolyse van talus, patella en os scaphoideum (aandoening)
	syndroom van osteolyse van talus, patella en os scaphoideum
	syndroom van Singh-Williams-McAlister
	Talo-patello-scaphoid osteolysis syndrome
	Singh Williams McAlister syndrome
	An extremely rare form of primary osteolysis, described in two sisters to date, with characteristics of bilateral osteolysis of the tali, scaphoids, and patellae (accompanied by periarticular swelling and pain) and short fourth metacarpals in the absence of renal disease. Autosomal recessive inheritance has been suggested.

Id	723580007
Status	Primitive

Associated morphology	abnormaal korte groei
Finding site	gehele bot van os metacarpi IV
Occurrence	congenitaal
Pathological process	proces van pathologische ontwikkeling

Associated morphology	osteolyse
Finding site	botstructuur van extremiteit
Occurrence	congenitaal
Pathological process	proces van pathologische ontwikkeling

DHD Diagnosis thesaurus reference set

RIVM authorized national diagnosis thesaurus to ICD10 complex mapping reference set

Target	M89.50
Term	Osteolyse van multipele lokalisaties

SNOMED CT to Orphanet simple map

50809

SNOMED CT to ICD-10 extended map

Target	M89.50
Rule	TRUE
Advice	ALWAYS M89.50
Correlation	SNOMED CT source code to target map code correlation not specified