Autosomal recessive hereditary disorder	Congenital microcephaly	Developmental hereditary disorder	Hereditary disorder of endocrine system	Hereditary metabolic disease	Mild intellectual disability	Secondary diabetes mellitus	Short stature disorder
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Primary microcephaly, mild intellectual disability, young-onset diabetes syndrome (disorder)
	Primary microcephaly, mild intellectual disability, young-onset diabetes syndrome
	A rare genetic syndromic intellectual disability disorder with characteristics of congenital, persistent microcephaly, low birth weight, short stature, childhood-onset seizures, global development delay, mild intellectual disability, and adolescent or young adult-onset diabetes mellitus. Gait ataxia, skeletal abnormalities, dorsocervical fat pad and infantile cirrhosis may also be associated. Brain morphology is typically normal, although delayed myelination and hypoplastic brainstem have been reported.
	syndroom van primaire microcefalie, lichte verstandelijke beperking en diabetes met aanvang op jonge leeftijd
	syndroom van primaire microcefalie, lichte mentale retardatie en diabetes met aanvang op jonge leeftijd syndroom van primaire microcefalie, lichte verstandelijke handicap en diabetes met aanvang op jonge leeftijd

Id	782755007
Status	Primitive

Associated morphology	Congenital smallness
Finding site	Head structure
Occurrence	Congenital
Pathological process	Pathological developmental process

Finding site

Structure of endocrine system

Has interpretation	Below reference range
Interprets	Height / growth measure

Has interpretation	Below reference range
Interprets	Birth head circumference

DHD Diagnosis thesaurus reference set

ICD-10 complex map reference set

Target	Q87.8
Rule	TRUE
Advice	ALWAYS Q87.8 \| POSSIBLE REQUIREMENT FOR ADDITIONAL CODE TO FULLY DESCRIBE DISEASE OR CONDITION
Correlation	SNOMED CT source code to target map code correlation not specified