genetische verstandelijke beperking	hereditaire ontwikkelingsstoornis	X-gebonden hereditaire recessieve aandoening
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X-gebonden mentale retardatie door PQBP1-mutatie (aandoening)
	X-gebonden mentale retardatie door PQBP1-mutatie
	X-gebonden mentale retardatie Renpenning-type syndroom van Renpenning
	Renpenning syndrome
	Porteous syndrome Sutherland-Haan syndrome Golabi-Ito-Hall syndrome X-linked intellectual deficit due to PQBP1 mutation Hamel cerebropalatocardiac syndrome

Id	699669001
Status	Primitive

Pathological process

proces van pathologische ontwikkeling

Has interpretation	gestoord
Interprets	intellectueel vermogen

Has interpretation	gestoord
Interprets	Adaptation behavior

SNOMED CT to Orphanet simple map

RIVM authorized national diagnosis thesaurus to ICD10 complex mapping reference set

Target	Q87.5
Term	Overige congenitale gestoorde-ontwikkelingssyndromen met overige skeletveranderingen

SNOMED CT to ICD-10 extended map

Target	F88
Rule	TRUE
Advice	ALWAYS F88 \| POSSIBLE REQUIREMENT FOR ADDITIONAL CODE TO FULLY DESCRIBE DISEASE OR CONDITION
Correlation	SNOMED CT source code to target map code correlation not specified