Autosomal dominant hereditary disorder	Craniosynostosis syndrome	Developmental hereditary disorder	Disorder of skull	Hereditary disorder of musculoskeletal system	Multiple malformation syndrome with facial-limb defects as major feature
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Craniosynostosis Boston type (disorder)
	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.
	craniosynostose Boston-type
	syndroom van Warman-Mulliken-Hayward craniosynostose Warman-type CSB

Id	720817008
Status	Primitive

Associated morphology	Morphologically abnormal structure
Finding site	Face structure
Occurrence	Congenital
Pathological process	Pathological developmental process

Associated morphology	Morphologically abnormal structure
Finding site	Limb structure
Occurrence	Congenital
Pathological process	Pathological developmental process

Associated morphology	Congenital premature fusion
Finding site	Joint structure of suture of skull
Occurrence	Congenital
Pathological process	Pathological developmental process

Finding site	Bone structure of cranium
Pathological process	Pathological developmental process

DHD Diagnosis thesaurus reference set

ICD-10 complex map reference set

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