Developmental hereditary disorder	Intellectual disability	X-linked recessive hereditary disease
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Renpenning syndrome (disorder)
	Renpenning syndrome
	Porteous syndrome Sutherland-Haan syndrome Golabi-Ito-Hall syndrome X-linked intellectual deficit due to PQBP1 mutation Hamel cerebropalatocardiac syndrome
	X-gebonden mentale retardatie door PQBP1-mutatie
	syndroom van Renpenning X-gebonden mentale retardatie Renpenning-type

Id	699669001
Status	Primitive

Pathological process

Pathological developmental process

DHD Diagnosis thesaurus reference set

ICD-10 complex map reference set

Target	Q87.5
Rule	TRUE
Advice	ALWAYS Q87.5
Correlation	SNOMED CT source code to target map code correlation not specified