Cardiac arrhythmia associated with genetic disorder	Cardiovascular system hereditary disorder	Developmental hereditary disorder	Intellectual disability	X-linked recessive hereditary disease
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X-linked intellectual disability, cardiomegaly, congestive heart failure syndrome (disorder)
	X-linked intellectual disability, cardiomegaly, congestive heart failure syndrome
	A rare X-linked syndromic intellectual disability disorder with characteristics of profound intellectual disability, global developmental delay with absent speech, seizures, large joint contractures, abnormal position of thumbs and middle-age onset of cardiomegaly and atrioventricular valve abnormalities, resulting in subsequent congestive heart failure. Additional features include variable facial dysmorphism (notably large ears with over folded helix) and large testes. There is evidence the disease is caused by mutation in the CLIC2 gene on chromosome Xq28.
	X-gebonden syndroom van verstandelijke beperking, cardiomegalie en congestief hartfalen
	X-gebonden syndroom van mentale retardatie, cardiomegalie en congestief hartfalen X-gebonden syndroom van verstandelijke handicap, cardiomegalie en congestief hartfalen

Id	773587008
Status	Primitive

Finding site

Heart structure

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