aandoening van sinus frontalis	autosomaal dominante hereditaire aandoening	congenitaal glaucoom	congenitale afwijking van neusbijholte	hereditaire aandoening van visueel systeem	hereditaire ontwikkelingsstoornis	microcornea
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syndroom van microcornea, glaucoom en afwezigheid van sinus frontalis (aandoening)
	syndroom van microcornea, glaucoom en afwezigheid van sinus frontalis
	Microcornea with glaucoma and absent frontal sinus syndrome
	A rare developmental defect during embryogenesis syndrome characterized by the association of microcornea, glaucoma and frontal sinus hypoplasia. Thick palmar skin and torus palatinus have also been reported. There have been no further descriptions in the literature since 1995.

Id	716166002
Status	Primitive

Associated morphology	afwezigheid
Finding site	structuur van sinus frontalis
Occurrence	congenitaal
Pathological process	proces van pathologische ontwikkeling

Associated morphology	afwijkend klein
Finding site	structuur van cornea
Occurrence	congenitaal
Pathological process	proces van pathologische ontwikkeling

DHD Diagnosis thesaurus reference set

RIVM authorized national diagnosis thesaurus to ICD10 complex mapping reference set

Target	Q15.0
Term	Congenitaal glaucoom

Target	Q13.4
Term	Overige congenitale misvormingen van cornea

Target	Q34.8
Term	Overige gespecificeerde congenitale misvormingen van ademhalingsstelsel

SNOMED CT to Orphanet simple map

2536

SNOMED CT to ICD-10 extended map

Target	Q15.8
Rule	TRUE
Advice	ALWAYS Q15.8 \| POSSIBLE REQUIREMENT FOR ADDITIONAL CODE TO FULLY DESCRIBE DISEASE OR CONDITION
Correlation	SNOMED CT source code to target map code correlation not specified