congenitale macrocefalie	dwerggroei	hereditaire ontwikkelingsstoornis	verstandelijke beperking	X-gebonden hereditaire dominante aandoening
\|	\|	\|	\|	\|

X-gebonden verstandelijke beperking type Atkin (aandoening)
	X-gebonden verstandelijke beperking type Atkin
	X-gebonden verstandelijke handicap type Atkin syndroom van Atkin-Flaitz X-gebonden mentale retardatie type Atkin
	Atkin Flaitz syndrome
	X-linked intellectual disability Atkin type
	Atkin-Flaitz syndrome has characteristics of moderate to severe intellectual deficit, short stature, macrocephaly, and characteristic facies. It has been described in 11 males and three females from three successive generations of the same family. The males also presented with postpubertal macroorchidism. Transmission is X-linked.

Id	718577005
Status	Primitive

Associated morphology	vergroting
Finding site	structuur van hoofd
Occurrence	congenitaal
Pathological process	proces van pathologische ontwikkeling

Interprets

meetbare observatie betreffende lengte en/of groei

Has interpretation	boven referentiebereik
Interprets	hoofdomtrek

Has interpretation	gestoord
Interprets	intellectueel vermogen

Has interpretation	gestoord
Interprets	Adaptation behavior

DHD Diagnosis thesaurus reference set

RIVM authorized national diagnosis thesaurus to ICD10 complex mapping reference set

Target	Q87.8
Term	Overige gespecificeerde congenitale gestoorde-ontwikkelingssyndromen, niet elders geclassificeerd

SNOMED CT to Orphanet simple map

1193

SNOMED CT to ICD-10 extended map

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