Autosomal dominant hereditary disorder	Brachydactyly	Congenital hallux varus	Developmental hereditary disorder	Hereditary disorder of musculoskeletal system	Intellectual disability	Multiple malformation syndrome with limb defect as major feature
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Brachydactyly and preaxial hallux varus syndrome (disorder)
	Brachydactyly and preaxial hallux varus syndrome
	The association of hallux varus with short thumbs and first toes (involving the metacarpals, metatarsals, and distal phalanges; the proximal and middle phalanges are of normal length) and abduction of the affected digits. The syndrome has been described in eight affected individuals from four successive generations of one family. Intellectual deficit was observed in all reported individuals. Transmission appears to be autosomal dominant.
	syndroom van brachydactylie en preaxiale hallux varus

Id	732957009
Status	Primitive

Associated morphology	Abnormally short growth
Finding site	Entire digit
Occurrence	Congenital
Pathological process	Pathological developmental process

Associated morphology	Varus deformity
Finding site	Joint of hallux
Occurrence	Congenital
Pathological process	Pathological developmental process

DHD Diagnosis thesaurus reference set

ICD-10 complex map reference set

Target	Q73.8
Rule	TRUE
Advice	ALWAYS Q73.8 \| POSSIBLE REQUIREMENT FOR ADDITIONAL CODE TO FULLY DESCRIBE DISEASE OR CONDITION
Correlation	SNOMED CT source code to target map code correlation not specified

Target	Q66.3
Rule	TRUE
Advice	ALWAYS Q66.3
Correlation	SNOMED CT source code to target map code correlation not specified