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syndroom van telecanthus, hypertelorisme, strabisme en pes cavus (aandoening)
syndroom van telecanthus, hypertelorisme, strabisme en pes cavus
syndroom van telecanthus, hypertelorisme, strabismus en pes cavus
syndroom van Krauss-Herman-Holmes
Krauss-Herman-Holmes-syndroom
syndroom van telecanthus, hypertelorisme, scheelzien en holvoet
Telecanthus, hypertelorism, strabismus, pes cavus syndrome
Telecanthus-hypertelorism-strabismus-pes cavus syndrome is characterized by telecanthus, hypertelorism, strabismus, pes cavus and other variable anomalies. It has been described in a father and his son. The son also had hypospadias, bilateral inguinal hernia, clinodactyly and camptodactyly of the fingers, and radiographic findings including flared metaphyses of the long bones and osteopenia.
Id733067006
StatusPrimitive
Associated morphologyklauwvormige deformiteit
Finding sitestructuur van voet
Occurrencecongenitaal
Pathological processproces van pathologische ontwikkeling
DHD Diagnosis thesaurus reference set
RIVM authorized national diagnosis thesaurus to ICD10 complex mapping reference set
TargetQ10.3
TermOverige congenitale misvormingen van ooglid
TargetQ75.2
TermHypertelorisme
TargetH50.8
TermOverig gespecificeerd strabismus
TargetQ66.7
TermPes cavus
SNOMED CT to Orphanet simple map3293
SNOMED CT to ICD-10 extended map
TargetQ87.8
RuleTRUE
AdviceALWAYS Q87.8 | POSSIBLE REQUIREMENT FOR ADDITIONAL CODE TO FULLY DESCRIBE DISEASE OR CONDITION
CorrelationSNOMED CT source code to target map code correlation not specified