Autosomal dominant hereditary disorder	Congenital hepatomegaly	Congenital hyperplasia of muscle	Developmental hereditary disorder	Digestive system hereditary disorder	Hereditary disorder of musculoskeletal system	Multiple system malformation syndrome
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Muscular hypertrophy, hepatomegaly, polyhydramnios syndrome (disorder)
	Muscular hypertrophy, hepatomegaly, polyhydramnios syndrome
	A rare genetic disease with characteristics of symmetrical muscular hypertrophy, hepatomegaly, polyhydramnios, macrocephaly and mild delay in motor, speech and language development.
	syndroom van musculaire hypertrofie, hepatomegalie en polyhydramnion

Id	773584001
Status	Primitive

Associated morphology	Hyperplasia
Finding site	Skeletal muscle system structure
Occurrence	Congenital
Pathological process	Pathological developmental process

Associated morphology	Enlargement
Finding site	Entire liver
Occurrence	Congenital
Pathological process	Pathological developmental process

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