||||||
orofaciodigitaal syndroom type 5 (aandoening)
orofaciodigitaal syndroom type 5
OFD5
syndroom van postaxiale polydactylie en mediane splijting van bovenlip
orofaciodigitaal syndroom Thurston-type
syndroom van Thurston
Oro-facial digital syndrome type 5
Thurston syndrome
Orofaciodigital syndrome Thurston type
Orofaciodigital syndrome type 5
Syndrome with characteristics of median cleft of upper lip, postaxial polydactyly of hands and feet and oral manifestations (duplicated frenulum). Less than 20 patients (predominantly of Indian origin) have been reported so far. Autosomal recessive inheritance has been suggested, but the causative gene has not yet been identified.
Id722105002
StatusPrimitive
Associated morphologymorfologische afwijking
Finding sitestructuur van huid
Occurrencecongenitaal
Pathological processproces van pathologische ontwikkeling
Associated morphologydysplasie
Finding sitestructuur van ectoderm
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