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obesitas door genetisch bepaalde leptinereceptordeficiëntie (aandoening)
obesitas door genetisch bepaalde leptinereceptordeficiëntie
obesitas door mutatie in gen voor leptinereceptor
Obesity due to leptin receptor gene deficiency
A rare, genetic, non-syndromic, obesity disease characterized by severe, early-onset obesity, associated with major hyperphagia and endocrine abnormalities, resulting from leptin receptor deficiency.
Id785722006
StatusPrimitive
SNOMED CT to Orphanet simple map179494
SNOMED CT to ICD-10 extended map
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