autosomaal dominante hereditaire aandoening	congenitale hypoplastische anemie	hereditair tumorpredispositiesyndroom	hereditaire aandoening van cellulair component van bloed	hereditaire ontwikkelingsstoornis
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primaire rodebloedcelaplasie (aandoening)
	primaire rodebloedcelaplasie
	BDA erythrogenesis imperfecta hypoplastische congenitale anemie syndroom van Aase Diamond-Blackfan-anemie DBA Aase-Smith-syndroom type II congenitale hypoplastische anemie Blackfan-Diamond-anemie
	Aase syndrome
	Aase Smith II syndrome Blackfan-Diamond anemia Congenital pure red cell aplasia Congenital hypoplastic anemia Blackfan-Diamond type

Id	71988008
Status	Primitive

Associated morphology	hypoplasie
Finding site	structuur van beenmerg
Occurrence	congenitaal
Pathological process	proces van pathologische ontwikkeling

Has interpretation	onder referentiebereik
Interprets	telling van erytrocyten

Has interpretation	onder referentiebereik
Interprets	Measurement of total hemoglobin concentration

Due to

verlaagde aanmaak van erytrocyten

DHD Diagnosis thesaurus reference set

SNOMED CT to Orphanet simple map

124

SNOMED CT to ICD-10 extended map

Target	D61.0
Rule	TRUE
Advice	ALWAYS D61.0
Correlation	SNOMED CT source code to target map code correlation not specified