Congenital hypergonadotropic hypogonadism	Intellectual disability	Multiple malformation syndrome with facial defects as major feature	Multiple malformation syndrome with facial defects as major feature	Primary hypogonadism	Type 1 diabetes mellitus	Type 1 diabetes mellitus
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Intellectual disability, craniofacial dysmorphism, hypogonadism, diabetes mellitus syndrome (disorder)
	Intellectual disability, craniofacial dysmorphism, hypogonadism, diabetes mellitus syndrome
	Mental retardation syndrome Belgian type
	This syndrome has characteristics of moderate intellectual deficit, craniofacial dysmorphism, hypergonadotropic hypogonadism, eunuchoid habitus, type 1 diabetes mellitus, and epilepsy. It has been described in four patients (three brothers and their sister). This syndrome is probably transmitted as an autosomal recessive trait.
	syndroom van verstandelijke beperking, craniofaciale dysmorfie, hypogonadisme en diabetes mellitus
	syndroom van verstandelijke beperking, craniofaciale dysmorfie, hypogenitalisme en diabetes mellitus

Id	722454003
Status	Primitive

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

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

DHD Diagnosis thesaurus reference set

ICD-10 complex map reference set

Target	Q87.0
Rule	TRUE
Advice	ALWAYS Q87.0 \| POSSIBLE REQUIREMENT FOR ADDITIONAL CODE TO FULLY DESCRIBE DISEASE OR CONDITION
Correlation	SNOMED CT source code to target map code correlation not specified