autosomaal hereditaire aandoening	congenitale afwijking van perifere zenuw	congenitale afwijking van zenuwstelsel van hoofd en/of hals	congenitale uitval van nervus facialis	hereditaire aandoening van zenuwstelsel	hereditaire ontwikkelingsstoornis
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geïsoleerde hereditaire congenitale faciale paralyse (aandoening)
	geïsoleerde hereditaire congenitale faciale paralyse
	Isolated hereditary congenital facial paralysis
	An extremely rare neurological disorder presumed to result from maldevelopment of the facial nucleus and/or cranial nerve reported in fewer than 10 families to date. It manifests as non-progressive, isolated, unilateral or bilateral, symmetrical or asymmetrical facial palsy. Involvement of the branches of the facial nerve can be unequal.

Id	733091002
Status	Primitive

Has interpretation	afwezig
Interprets	Movement observable

Associated morphology	aplasia
Finding site	structuur van nervus facialis
Occurrence	congenitaal
Pathological process	proces van pathologische ontwikkeling

Interprets

DHD Diagnosis thesaurus reference set

RIVM authorized national diagnosis thesaurus to ICD10 complex mapping reference set

Target	Q87.0
Term	Congenitale gestoorde-ontwikkelingssyndromen waarbij voornamelijk aangezicht is aangedaan

SNOMED CT to Orphanet simple map

306527

SNOMED CT to ICD-10 extended map

Target	Q87.0
Rule	TRUE
Advice	ALWAYS Q87.0 \| POSSIBLE REQUIREMENT FOR ADDITIONAL CODE TO FULLY DESCRIBE DISEASE OR CONDITION
Correlation	SNOMED CT source code to target map code correlation not specified