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obesitas door mutatie in gen voor leptinereceptor (aandoening)
obesitas door mutatie in gen voor leptinereceptor
obesitas door genetisch bepaalde leptinereceptordeficiëntie
Obesity due to leptin receptor gene deficiency
A rare genetic non-syndromic obesity disease with characteristics of severe early-onset obesity associated with major hyperphagia and endocrine abnormalities resulting from leptin receptor deficiency. Caused by homozygous mutation in the gene encoding the leptin receptor (LEPR) on chromosome 1p31.
Id785722006
StatusPrimitive
referentieset met complexe 'mapping' naar ICD-10
TargetE66.8
RuleTRUE
AdviceALWAYS E66.8 | POSSIBLE REQUIREMENT FOR ADDITIONAL CODE TO FULLY DESCRIBE DISEASE OR CONDITION
CorrelationSNOMED CT source code to target map code correlation not specified