Autosomal dominant hereditary disorder	Robinow syndrome
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Autosomal dominant Robinow syndrome (disorder)
	Autosomal dominant Robinow syndrome
	The more common type of Robinow syndrome characterized by mild to moderate limb shortening and abnormalities of the head, face and external genitalia.
	autosomaal dominant Robinow-syndroom
	autosomaal dominant syndroom van Robinow

Id	890233009
Status	Defined

Clinical course

Associated morphology	Dysplasia
Finding site	Skeletal system structure
Occurrence	Congenital
Pathological process	Pathological developmental process

Associated morphology	Abnormally short growth
Finding site	Musculoskeletal structure of limb
Occurrence	Congenital
Pathological process	Pathological developmental process

Associated morphology	Aplasia
Finding site	Bone structure of spine
Occurrence	Congenital
Pathological process	Pathological developmental process

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

Interprets

Height / growth measure

ICD-10 complex map reference set

Target	Q87.1
Rule	TRUE
Advice	ALWAYS Q87.1 \| POSSIBLE REQUIREMENT FOR ADDITIONAL CODE TO FULLY DESCRIBE DISEASE OR CONDITION
Correlation	SNOMED CT source code to target map code correlation not specified