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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.
Id773345007
StatusPrimitive
Associated morphologyafwezigheid
Finding sitegeheel gebitselement
Occurrencecongenitaal
Pathological processproces van pathologische ontwikkeling
referentieset met complexe 'mapping' naar ICD-10
TargetK00.0
RuleTRUE
AdviceALWAYS K00.0 | POSSIBLE REQUIREMENT FOR ADDITIONAL CODE TO FULLY DESCRIBE DISEASE OR CONDITION
CorrelationSNOMED CT source code to target map code correlation not specified