Autosomal dominant hereditary disorder	Congenital abnormality of skull shape	Congenital anomaly of bone and joint	Craniosynostosis syndrome	Developmental hereditary disorder	Hereditary disorder of musculoskeletal system	Multiple malformation syndrome with limb defect as major feature	Syndactyly
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Craniosynostosis Philadelphia type (disorder)
	Craniosynostosis Philadelphia type
	A form of syndromic craniosynostosis with characteristics of sagittal/dolichocephalic head shape with a relatively normal facial appearance and complete soft tissue syndactyly of hand and foot. Transmission is autosomal dominant with variable expression of the hand findings, and incomplete penetrance of the sagittal craniosynostosis.
	craniosynostose Philadelphia-type

Id	720818003
Status	Primitive

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

Associated morphology	Abnormal shape
Finding site	Bone structure of cranium
Occurrence	Congenital
Pathological process	Pathological developmental process

Associated morphology	Congenital abnormal fusion
Finding site	Digit structure
Occurrence	Congenital
Pathological process	Pathological developmental process

DHD Diagnosis thesaurus reference set

ICD-10 complex map reference set

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