coloboom van fundus oculi	lenticonus posterior	microcornea
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syndroom van microcornea, posterieure megalolenticonus, persisterende foetale vasculatuur en coloboom (aandoening)
	syndroom van microcornea, posterieure megalolenticonus, persisterende foetale vasculatuur en coloboom
	syndroom van microcornea, megalolenticonus posterior, persistente foetale vasculatuur en coloboom
	Microcornea, posterior megalolenticonus, persistent fetal vasculature, coloboma syndrome
	MPPC (microcornea, posterior megalolenticonus, persistent fetal vasculature, coloboma) syndrome
	A rare developmental defect of the eye characterized by bilateral microcornea, posterior megalolenticonus, persistent fetal vasculature (extending from the posterior pole of the lens to the optic disc) and posterior chorioretinal coloboma.

Id	773690008
Status	Primitive

Associated morphology	afwijkende vorm
Finding site	structuur van achterste oppervlak van lens
Occurrence	congenitaal
Pathological process	proces van pathologische ontwikkeling

Associated morphology	fusiedefect door stoornis in ontwikkeling
Finding site	structuur van fundus oculi
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	Q15.8
Term	Overige gespecificeerde congenitale misvormingen van oog

SNOMED CT to Orphanet simple map

231736

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