Congenital hypogonadotropic hypogonadism	Genetic disease	Multiple malformation syndrome with facial defects as major feature	Multiple malformation syndrome with unusual brain and/or neuromuscular findings	Obesity
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Prader-Willi-like syndrome (disorder)
	Prader-Willi-like syndrome
	A rare genetic, endocrine disease with manifestations of a Prader-Willi syndrome phenotype (including obesity, hyperphagia, hypotonia, psychomotor delay, intellectual disability, small hands/feet, hypogonadism, growth hormone deficiency and characteristic facial features) occurring in the absence of 15q11-q13 genomic abnormalities.
	Prader-Willi-achtig syndroom
	PWLS Prader-Willi-'like' syndroom

Id	770680004
Status	Primitive

Finding site	Structure of distal part of pituitary
Occurrence	Congenital
Pathological process	Pathological developmental process

Has interpretation	Above reference range
Interprets	Body weight measure

Finding site	Gonadal endocrine structure
Occurrence	Congenital
Pathological process	Pathological developmental process

Associated morphology	Morphologically abnormal structure
Finding site	Face structure
Occurrence	Congenital
Pathological process	Pathological developmental process

ICD-10 complex map reference set

Target	Q87.1
Rule	TRUE
Advice	ALWAYS Q87.1 \| POSSIBLE REQUIREMENT FOR ADDITIONAL CODE TO FULLY DESCRIBE DISEASE OR CONDITION
Correlation	SNOMED CT source code to target map code correlation not specified

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6q16 microdeletion syndrome

MAGEL2-related Prader-Willi-like syndrome

SIM1-related Prader-Willi-like syndrome