autosomaal recessieve hereditaire aandoening	hereditaire aandoening van cardiovasculair systeem	hereditaire aandoening van erytrocyt	hereditaire aandoening van integumentum	hereditaire aandoening van trombocyt	trombotische trombocytopenische purpura
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syndroom van familiaire trombotische trombocytopenische purpura en hemolytische uremie (aandoening)
	syndroom van familiaire trombotische trombocytopenische purpura en hemolytische uremie
	familiaire trombotische trombocytopenische purpura en trombotische microangiopathie familiaire TTP-TMA familiaire TTP-HUS syndroom van Upshaw-Schulman Upshaw-Schulman-syndroom
	Upshaw-Schulman syndrome
	Congenital ADAMTS-13 deficiency Familial TTP/HUS Familial thrombotic thrombocytopenic purpura / hemolytic uremic syndrome

Id	373420004
Status	Primitive

Has interpretation	onder referentiebereik
Interprets	telling van erytrocyten

Has interpretation	onder referentiebereik
Interprets	Measurement of total hemoglobin concentration

Finding site

Associated morphology

Has interpretation	afwijkend
Interprets	hemostase

Has interpretation	onder referentiebereik
Interprets	Platelet count

Has interpretation	aanwezig
Interprets	hemolyse

Associated morphology	purpura
Finding site	structuur van huid

Associated morphology	microtrombus
Finding site	structuur van arteriola

Associated morphology	microtrombus
Finding site	structuur van capillair

SNOMED CT to Orphanet simple map

93583

SNOMED CT to ICD-10 extended map

Target	M31.1
Rule	TRUE
Advice	ALWAYS M31.1 \| POSSIBLE REQUIREMENT FOR ADDITIONAL CODE TO FULLY DESCRIBE DISEASE OR CONDITION
Correlation	SNOMED CT source code to target map code correlation not specified