Autosomal recessive hereditary disorder	Congenital anomaly of skull	Developmental hereditary disorder	Dysplasia with increased bone density	Hereditary disorder of musculoskeletal system
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Cranioosteoarthropathy (disorder)
	Cranioosteoarthropathy
	Currarino disease Currarino idiopathic osteoarthropathy Reginato Schiapachasse syndrome Cranio-osteoarthropathy
	A form of primary hypertrophic osteoarthropathy with characteristics of delayed closure of the cranial sutures and fontanelles, digital clubbing, arthropathy, and periostosis. To date, about 30 cases have been reported. May also be associated with congenital heart disease. It is caused by mutations in the HPGD gene (4q33-q34) and is inherited as an autosomal recessive trait.
	cranio-osteoartropathie
	ziekte van Currarino syndroom van Reginato-Schiapachasse

Id	720753002
Status	Primitive

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

Has interpretation	Above reference range
Interprets	Bone density scan

ICD-10 complex map reference set

Target	M89.48
Rule	TRUE
Advice	ALWAYS M89.48 \| POSSIBLE REQUIREMENT FOR ADDITIONAL CODE TO FULLY DESCRIBE DISEASE OR CONDITION
Correlation	SNOMED CT source code to target map code correlation not specified