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syndroom van niet doorkomen van tanden, hypoplasie van maxilla en genu valgum (aandoening)
syndroom van niet doorkomen van tanden, hypoplasie van maxilla en genu valgum
syndroom van niet doorkomen van tanden, hypoplasie van maxillaire en genu valgum
syndroom van Stoelinga-De Koomen-Davis
Non-eruption of teeth, maxillary hypoplasia, genu valgum syndrome
Stoelinga de Koomen Davis syndrome
An extremely rare syndrome with characteristics of multiple unerupted permanent teeth, hypoplasia of the alveolar process and of the maxillo-zygomatic region, severe genu valgum and deformed ears. Consanguinity in the family suggested autosomal recessive inheritance.
Id723442008
StatusPrimitive
Associated morphologyhypoplasie
Finding sitebotstructuur van kaak
Occurrencecongenitaal
Pathological processproces van pathologische ontwikkeling
Associated morphologyvalgusmisvorming
Finding sitestructuur van kniegewricht
Occurrencecongenitaal
Pathological processproces van pathologische ontwikkeling
referentieset met complexe 'mapping' naar ICD-10
TargetK00.6
RuleTRUE
AdviceALWAYS K00.6 | POSSIBLE REQUIREMENT FOR ADDITIONAL CODE TO FULLY DESCRIBE DISEASE OR CONDITION
CorrelationSNOMED CT source code to target map code correlation not specified
TargetK07.0
RuleTRUE
AdviceALWAYS K07.0
CorrelationSNOMED CT source code to target map code correlation not specified
TargetQ74.1
RuleTRUE
AdviceALWAYS Q74.1
CorrelationSNOMED CT source code to target map code correlation not specified