Autosomal recessive hereditary disorder	Congenital hypogonadotropic hypogonadism	Hereditary disorder of endocrine system	Hereditary disorder of nervous system	Reproductive system hereditary disorder	Severe obesity
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Obesity due to leptin receptor gene deficiency (disorder)
	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.
	obesitas door genetisch bepaalde leptinereceptordeficiëntie
	obesitas door mutatie in gen voor leptinereceptor

Id	785722006
Status	Primitive

Finding site	Gonadal endocrine structure
Occurrence	Congenital

Finding site	Structure of distal part of pituitary
Occurrence	Congenital

Has interpretation	Above reference range
Interprets	Body weight measure

ICD-10 complex map reference set

Target	E66.8
Rule	TRUE
Advice	ALWAYS E66.8 \| POSSIBLE REQUIREMENT FOR ADDITIONAL CODE TO FULLY DESCRIBE DISEASE OR CONDITION
Correlation	SNOMED CT source code to target map code correlation not specified