bevinding betreffende grove beweging van lichaam en extremiteiten
congenitaal hypogonadotroop hypogonadisme
congenitale uitval van nervus facialis
motorische uitval
perifere axonale neuropathie
uitval van nervus
||||||
syndroom van Möbius-syndroom, axonale neuropathie, hypogonadotropisch hypogonadisme (aandoening)
syndroom van Möbius-syndroom, axonale neuropathie, hypogonadotropisch hypogonadisme
syndroom van syndroom van Möbius, axonale neuropathie, hypogonadotropisch hypogonadisme
syndroom van möbiussyndroom, axonale neuropathie, hypogonadotropisch hypogonadisme
Moebius syndrome, axonal neuropathy, hypogonadotropic hypogonadism syndrome
A rare syndromic neurological disorder characterized by the association of Möbius syndrome (congenital facial palsy with impaired ocular abduction) with peripheral axonal neuropathy and hypogonadotropic hypogonadism. There have been no further reports since 1996.
Id724174003
StatusPrimitive
Finding sitestructuur van nervus facialis
Occurrencecongenitaal
Finding siteendocriene structuur van gonade
Occurrencecongenitaal
Finding sitestructuur van pars distalis adenohypophysis
Occurrencecongenitaal
Has interpretationafwezig
Interpretsgrove beweging van lichaam en extremiteiten
InterpretsMovement
Finding sitestructuur van axon
DHD Diagnosis thesaurus reference set
RIVM authorized national diagnosis thesaurus to ICD10 complex mapping reference set
TargetQ87.0
TermCongenitale gestoorde-ontwikkelingssyndromen waarbij voornamelijk aangezicht is aangedaan
SNOMED CT to Orphanet simple map2560
SNOMED CT to ICD-10 extended map
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
TargetG60.8
RuleTRUE
AdviceALWAYS G60.8
CorrelationSNOMED CT source code to target map code correlation not specified
TargetE23.0
RuleTRUE
AdviceALWAYS E23.0
CorrelationSNOMED CT source code to target map code correlation not specified