autosomaal recessieve hereditaire aandoening	congenitale afwijking van haar	fotodermatose	genetische verstandelijke beperking	hereditaire aandoening van integumentum	hereditaire ontwikkelingsstoornis	malformatiesyndroom met betrokkenheid van meerdere systemen
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syndroom van haarafwijking, fotosensitiviteit en verstandelijke beperking (aandoening)
	syndroom van haarafwijking, fotosensitiviteit en verstandelijke beperking
	syndroom van Calderón-González-Cantu syndroom van haarafwijking, fotosensitiviteit en verstandelijke handicap syndroom van haarafwijking, fotosensitiviteit en mentale retardatie
	Hair defect with photosensitivity and intellectual disability syndrome
	Calderón González Cantu syndrome
	Syndrome with the association of stubby, coarse, sparse and fragile hair, eyebrows and eyelashes with photosensitivity and nonprogressive intellectual deficit, without a demonstrable metabolic aberration. It has been described in three sisters born to consanguineous parents.

Id	721007005
Status	Primitive

Causative agent	licht
Finding site	structuur van huid

Associated morphology	morfologische afwijking
Finding site	structuur van haar
Occurrence	congenitaal
Pathological process	proces van pathologische ontwikkeling

Has interpretation	gestoord
Interprets	intellectueel vermogen

Has interpretation	gestoord
Interprets	Adaptation behavior

Has interpretation

SNOMED CT to ICD-10 extended map

Target	Q84.2
Rule	TRUE
Advice	ALWAYS Q84.2 \| POSSIBLE REQUIREMENT FOR ADDITIONAL CODE TO FULLY DESCRIBE DISEASE OR CONDITION
Correlation	SNOMED CT source code to target map code correlation not specified

Target	L56.8
Rule	TRUE
Advice	ALWAYS L56.8
Correlation	SNOMED CT source code to target map code correlation not specified

Target	F79.9
Rule	TRUE
Advice	ALWAYS F79.9
Correlation	SNOMED CT source code to target map code correlation not specified