Developmental hereditary disorder	Intellectual disability	X-linked hereditary disease
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X-linked intellectual disability Wilson type (disorder)
	X-linked intellectual disability Wilson type
	This syndrome has characteristics of severe intellectual deficit with mutism, epilepsy, growth retardation and recurrent infections. It has been described in three males from three generations of one family. The causative gene has been located to the 11p region of the X chromosome.
	X-gebonden verstandelijke beperking Wilson-type
	X-gebonden verstandelijke handicap Wilson-type X-gebonden mentale retardatie Wilson-type

Id	719009006
Status	Primitive

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