aandoening van schedel	autosomaal dominante hereditaire aandoening	craniosynostose	hereditaire aandoening van bewegingsapparaat	hereditaire ontwikkelingsstoornis	polymalformatief syndroom met defect van aangezicht en extremiteit als voornaamst kenmerk
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craniosynostose Boston-type (aandoening)
	craniosynostose Boston-type
	craniosynostose Warman-type CSB syndroom van Warman-Mulliken-Hayward
	Craniosynostosis Boston type
	Craniosynostosis Warman type Warman Mulliken Hayward syndrome
	A form of syndromic craniosynostosis with characteristics of highly variable craniosynostosis with frontal bossing, turribrachycephaly and cloverleaf skull anomaly. Hypoplasia of the supraorbital ridges, cleft palate, extra teeth and limb anomalies has also been described. Associated problems include headache, poor vision, and seizures. Intelligence is normal.

Id	720817008
Status	Primitive

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

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

Associated morphology	premature fusie
Finding site	structuur van sutura cranii
Occurrence	congenitaal
Pathological process	proces van pathologische ontwikkeling

Finding site	botstructuur van cranium
Pathological process	proces van pathologische ontwikkeling

DHD Diagnosis thesaurus reference set

RIVM authorized national diagnosis thesaurus to ICD10 complex mapping reference set

Target	Q75.8
Term	Overige gespecificeerde congenitale misvormingen van schedel- en aangezichtsbeenderen

SNOMED CT to Orphanet simple map

1541

SNOMED CT to ICD-10 extended map

Target	Q75.8
Rule	TRUE
Advice	ALWAYS Q75.8 \| POSSIBLE REQUIREMENT FOR ADDITIONAL CODE TO FULLY DESCRIBE DISEASE OR CONDITION
Correlation	SNOMED CT source code to target map code correlation not specified