Acanthosis nigricans	Autosomal dominant hereditary disorder	Congenital anomaly of skin	Craniosynostosis syndrome	Developmental hereditary disorder	Hereditary disorder of musculoskeletal system	Inherited disorder of keratinization
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Cutis gyrata syndrome of Beare and Stevenson (disorder)
	Cutis gyrata syndrome of Beare and Stevenson
	Cutis gyrata, acanthosis nigricans, craniosynostosis syndrome Beare-Stevenson cutis gyrata syndrome
	syndroom van cutis gyrata, acanthosis nigricans en craniosynostose
	Beare-Stevenson-syndroom syndroom van Beare-Stevenson syndroom van cutis gyrata van Beare en Stevenson

Id	703528008
Status	Primitive

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

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

Has interpretation	Abnormal
Interprets	Keratinization

ICD-10 complex map reference set

Target	Q87.8
Rule	TRUE
Advice	ALWAYS Q87.8
Correlation	SNOMED CT source code to target map code correlation not specified