|||||||||
syndroom van trigonocefalie en brede digiti I (aandoening)
syndroom van trigonocefalie en brede digiti I
syndroom van trigonocefalie en brede duimen
syndroom van Hunter-Rudd-Hoffmann
Trigonocephaly with broad thumb syndrome
Hunter Rudd Hoffmann syndrome
This syndrome has characteristics of neonatal trigonocephaly and multiple anomalies including craniosynostosis, shallow orbits, unusual nose, deviation of the terminal phalanges of fingers and broad toes with duplication of the terminal phalanx. It has been described in a mother and her son. It is transmitted as an autosomal dominant trait.
Id719949001
StatusPrimitive
Associated morphologymorfologische afwijking
Finding sitestructuur van neus
Occurrencecongenitaal
Pathological processproces van pathologische ontwikkeling
Associated morphologyafwijkende vorm
Finding sitestructuur van os frontale
Occurrencecongenitaal
Pathological processproces van pathologische ontwikkeling
referentieset met complexe 'mapping' naar ICD-10
TargetQ87.0
RuleTRUE
AdviceALWAYS Q87.0 | POSSIBLE REQUIREMENT FOR ADDITIONAL CODE TO FULLY DESCRIBE DISEASE OR CONDITION
CorrelationSNOMED CT source code to target map code correlation not specified