congenitale ziekte	hereditaire aandoening van endocrien systeem	hereditaire aandoening van voortplantingsstelsel	hereditaire ontwikkelingsstoornis	hypogonadisme	obesitas	verstandelijke beperking	X-gebonden hereditaire recessieve aandoening
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syndromale X-gebonden verstandelijke beperking type 7 (aandoening)
	syndromale X-gebonden verstandelijke beperking type 7
	X-gebonden verstandelijke handicap type Ahmad syndromale X-gebonden mentale retardatie type 7
	Syndromic X-linked intellectual disability type 7
	X-linked intellectual disability Ahmad type
	A rare, X-linked syndromic intellectual disability disorder characterized by mild to moderate intellectual disability, obesity, hypogonadism, tapering fingers and microphallus with small or undescended testes, localized to Xp11.3-Xq23. Additional variable manifestations include alopecia, dental and eyesight anomalies, speech disabilities, and decreased body strength.

Id	719160009
Status	Primitive

Finding site	endocriene structuur van gonade
Occurrence	congenitaal

Has interpretation	boven referentiebereik
Interprets	meetbare observatie betreffende lichaamsgewicht

Pathological process

proces van pathologische ontwikkeling

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

85274

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