Autosomal dominant hereditary disorder	Developmental hereditary disorder	Dysostosis	Hereditary disorder of musculoskeletal system	Macrodactyly of toe	Multiple malformation syndrome with early overgrowth	Perodactylia of great toe
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Tall stature, scoliosis, macrodactyly of great toe syndrome (disorder)
	Tall stature, scoliosis, macrodactyly of great toe syndrome
	Tall stature, scoliosis, macrodactyly of hallux syndrome
	A rare genetic overgrowth or tall stature syndrome with skeletal involvement and characteristics of early and proportional overgrowth, osteopenia, lumbar scoliosis, arachnodactyly of the hands and feet, macrodactyly of the hallux, coxa valga with epiphyseal dysplasia of the femoral capital epiphyses and susceptibility to slipped capital femoral epiphysis. There is evidence the disease is caused by heterozygous mutation in the NPR2 gene on chromosome 9p13.
	syndroom van grote gestalte, scoliose en macrodactylie van grote teen
	syndroom van grote gestalte, scoliose en macrodactylie van hallux

Id	770788000
Status	Primitive

Associated morphology	Hypertrophy
Finding site	Hallux structure
Occurrence	Congenital
Pathological process	Pathological developmental process

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

DHD Diagnosis thesaurus reference set

ICD-10 complex map reference set

Target	Q87.3
Rule	TRUE
Advice	ALWAYS Q87.3 \| POSSIBLE REQUIREMENT FOR ADDITIONAL CODE TO FULLY DESCRIBE DISEASE OR CONDITION
Correlation	SNOMED CT source code to target map code correlation not specified