Arthrogryposis
Multiple malformation syndrome with unusual brain and/or neuromuscular findings
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Amyoplasia congenita disruptive sequence (disorder)
Amyoplasia congenita disruptive sequence
Myophagism congenita
Myodystrophia foetalis deformans
Classic arthrogryposis
Myodystrophia fetalis deformans
Congenital arthromyodysplasia
Amyoplasia congenita
amyoplasia congenita
congenitale amyoplasie
amyoplasia congenita
Id77016009
StatusPrimitive
Associated morphologyContracture
Finding siteStructure of joint region
OccurrenceCongenital
Pathological processPathological developmental process
Has interpretationDecreased
InterpretsRange of joint movement
Dutch rare neuromuscular disorders simple reference set
DHD Diagnosis thesaurus reference set
ICD-10 complex map reference set
TargetQ74.3
RuleTRUE
AdviceALWAYS Q74.3
CorrelationSNOMED CT source code to target map code correlation not specified
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Adducted thumbs and arthrogryposis syndrome Christian type
Arthrogryposis hyperkeratosis syndrome lethal form
Autosomal recessive myogenic arthrogryposis multiplex congenita
Congenital lethal myopathy Compton North type
Hypomyelination neuropathy arthrogryposis syndrome
Illum syndrome
Intellectual disability, developmental delay, contracture syndrome
Intellectual disability, developmental delay, contracture syndrome
Lethal arthrogryposis with anterior horn cell disease
Van den Ende-Gupta syndrome
X-linked distal arthrogryposis multiplex congenita