Autosomal dominant hereditary disorder	Congenital anomaly of nose	Developmental hereditary disorder	Multiple malformation syndrome with limb defect as major feature	Polysyndactyly
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Mirror hands and feet co-occurrent with nasal defect (disorder)
	Mirror hands and feet co-occurrent with nasal defect
	Laurin Sandrow syndrome Sandrow syndrome
	Complete polysyndactyly of the hands, mirror feet and nose anomalies (hypoplasia of the nasal alae and short columella), often associated with ulnar and/or fibular duplication (and sometimes tibial agenesis).
	Laurin-Sandrow-syndroom
	syndroom van Sandrow gespiegelde handen en voeten gelijktijdig met neusdefect syndroom van Laurin-Sandrow

Id	715440003
Status	Primitive

Associated morphology	Supernumerary structure
Finding site	Digit structure
Occurrence	Congenital
Pathological process	Pathological developmental process

Associated morphology	Morphologically abnormal structure
Finding site	Nasal structure
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	Q87.2
Rule	TRUE
Advice	ALWAYS Q87.2
Correlation	SNOMED CT source code to target map code correlation not specified