|||
adrenomyodystrofie (aandoening)
adrenomyodystrofie
Adrenomyodystrophy
An extremely rare genetic endocrine disease with characteristics of primary adrenal insufficiency, dystrophic myopathy, hepatic steatosis, severe psychomotor delay, megalocornea, failure to thrive, chronic constipation, and terminal bladder ectasia which can lead to death. There have been no further descriptions in the literature since 1982.
Id763311001
StatusPrimitive
referentieset met complexe 'mapping' naar ICD-10
TargetE27.4
RuleTRUE
AdviceALWAYS E27.4 | POSSIBLE REQUIREMENT FOR ADDITIONAL CODE TO FULLY DESCRIBE DISEASE OR CONDITION
CorrelationSNOMED CT source code to target map code correlation not specified