Autosomal recessive hereditary disorder	Congenital anomaly of visual system	Congenital macrocephaly	Developmental hereditary disorder	Disorder of eye region	Hereditary disorder of the visual system	Intellectual disability	Multiple malformation syndrome with early overgrowth	Obesity
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Macrocephaly, obesity, mental disability, ocular abnormality syndrome (disorder)
	MOMO syndrome
	Macrocephaly, obesity, mental disability, ocular abnormality syndrome MOMO (macrocephaly, obesity, mental disability, ocular abnormality) syndrome
	A very rare genetic overgrowth/obesity syndrome with characteristics of macrocephaly, obesity, mental (intellectual) disability and ocular abnormalities. Other frequent clinical signs include macrosomia, downslanting palpebral fissures, hypertelorism, broad nasal root, high and broad forehead and delay in bone maturation, in association with normal thyroid function and karyotype.
	syndroom van macrocefalie, obesitas, verstandelijke beperking en oogafwijking
	MOMO-syndroom syndroom van macrocefalie, obesitas, mentale retardatie en oogafwijking syndroom van macrocefalie, obesitas, verstandelijke handicap en oogafwijking

Id	724137002
Status	Primitive

Has interpretation	Above reference range
Interprets	Body weight measure

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

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

Has interpretation	Above reference range
Interprets	Head circumference

DHD Diagnosis thesaurus reference set

ICD-10 complex map reference set

Target	Q87.3
Rule	TRUE
Advice	ALWAYS Q87.3 \| POSSIBLE REQUIREMENT FOR ADDITIONAL CODE TO FULLY DESCRIBE DISEASE OR CONDITION
Correlation	SNOMED CT source code to target map code correlation not specified