|||||||
syndroom van alopecia, epilepsie en verstandelijke beperking type Moynahan (aandoening)
syndroom van alopecia, epilepsie en verstandelijke beperking type Moynahan
Alopecia, epilepsy, intellectual disability syndrome Moynahan type
Moynahan syndrome
A rare genetic epilepsy syndrome with characteristics of congenital alopecia, early-onset epilepsy, intellectual disability and speech delay. Large stature, delayed bone development and abnormal electroencephalogram have also been associated.
Id788417006
StatusPrimitive
Associated morphologycongenitale afwezigheid
Finding sitestructuur van pilus
Occurrencecongenitaal
Pathological processproces van pathologische ontwikkeling
referentieset met complexe 'mapping' naar ICD-10
TargetG40.4
RuleTRUE
AdviceALWAYS G40.4 | POSSIBLE REQUIREMENT FOR ADDITIONAL CODE TO FULLY DESCRIBE DISEASE OR CONDITION
CorrelationSNOMED CT source code to target map code correlation not specified