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coxoauriculair syndroom (aandoening)
coxoauriculair syndroom
Coxoauricular syndrome
An extremely rare primary bone defect described only in a mother and her three daughters to date. The disease has characteristics of short stature, hip dislocation, minor vertebral and pelvic changes and microtia with hearing loss. There have been no further descriptions in the literature since 1981.
Id732248005
StatusPrimitive
Associated morphologyafwijkend klein
Finding sitestructuur van auris externa
Occurrencecongenitaal
Pathological processproces van pathologische ontwikkeling
Associated morphologydysplasie
Finding sitebotstructuur
Occurrencecongenitaal
Pathological processproces van pathologische ontwikkeling
Associated morphologyluxatie
Finding sitestructuur van heupgewricht
Interpretsgehoorfunctie
DHD Diagnosis thesaurus reference set
SNOMED CT to Orphanet simple map1508
SNOMED CT to ICD-10 extended map
TargetQ87.1
RuleTRUE
AdviceALWAYS Q87.1 | POSSIBLE REQUIREMENT FOR ADDITIONAL CODE TO FULLY DESCRIBE DISEASE OR CONDITION
CorrelationSNOMED CT source code to target map code correlation not specified