Autosomal recessive hereditary disorder	Inherited arthrogryposis
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Lethal congenital contracture syndrome type 1 (disorder)
	Lethal congenital contracture syndrome type 1
	Herva disease Multiple contracture syndrome Finnish type
	An autosomal recessive disorder that is the most severe, neonatally lethal form of arthrogryposis a disorder characterized by congenital nonprogressive joint contractures. The contractures can involve the upper or lower limbs and/or the vertebral column, leading to various degrees of flexion or extension limitations evident at birth.
	letaal congenitaal contractuursyndroom type 1
	ziekte van Herva LCCS1 arthrogryposis multiplex congenita van Fins type

Id	715418007
Status	Primitive

Associated morphology	Contracture
Finding site	Structure of joint region
Occurrence	Congenital
Pathological process	Pathological developmental process

Has interpretation	Decreased
Interprets	Range of joint movement

DHD Diagnosis thesaurus reference set

ICD-10 complex map reference set

Target	Q68.8
Rule	TRUE
Advice	ALWAYS Q68.8
Correlation	SNOMED CT source code to target map code correlation not specified