afwezigheid van gebitselement door verstoorde ontwikkeling	autosomaal dominante hereditaire aandoening	hereditair tumorpredispositiesyndroom	oligodontie
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syndroom van oligodontie en predispositie voor maligne neoplasma (aandoening)
	syndroom van oligodontie en predispositie voor maligne neoplasma
	syndroom van oligodontie en predispositie voor maligniteit
	Oligodontia and cancer predisposition syndrome
	A rare genetic odontologic disease with characteristics of the congenital absence of six or more permanent teeth (excluding the third molars) in association with an increased risk for malignancies, ranging from gastrointestinal polyposis to early-onset colorectal cancer and/or breast cancer. Ectodermal dysplasia (manifesting with sparse hair and/or eyebrows) may also be associated.

Id	773345007
Status	Primitive

Associated morphology	afwezigheid
Finding site	structuur van gebitselementen
Occurrence	congenitaal
Pathological process	proces van pathologische ontwikkeling

Associated morphology	congenitaal afwijkend aantal
Finding site	structuur van gebitselement
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	K00.0
Term	Anodontie

SNOMED CT to Orphanet simple map

300576

SNOMED CT to ICD-10 extended map

Target	K00.0
Rule	TRUE
Advice	ALWAYS K00.0 \| POSSIBLE REQUIREMENT FOR ADDITIONAL CODE TO FULLY DESCRIBE DISEASE OR CONDITION
Correlation	SNOMED CT source code to target map code correlation not specified