Arthrogryposis
Developmental hereditary disorder
||
Inherited arthrogryposis (disorder)
Inherited arthrogryposis
hereditaire artrogrypose
erfelijke artrogrypose
Id28204005
StatusDefined
Associated morphologyContracture
Finding siteStructure of joint region
OccurrenceCongenital
Pathological processPathological developmental process
Has interpretationDecreased
InterpretsRange of joint movement
ICD-10 complex map reference set
TargetQ68.8
RuleTRUE
AdviceALWAYS Q68.8
CorrelationSNOMED CT source code to target map code correlation not specified
|
Aase Smith type 1 syndrome
Adducted thumbs and arthrogryposis syndrome Christian type
Arthrogryposis and ectodermal dysplasia syndrome
Autosomal recessive myogenic arthrogryposis multiplex congenita
Camptobrachydactyly
Congenital contractural arachnodactyly
Congenital lethal myopathy Compton North type
Contracture with ectodermal dysplasia and orofacial cleft syndrome
Distal arthrogryposis syndrome14
Familial arthrogryposis-cholestatic hepatorenal syndrome
German syndrome
Hereditary inclusion body myopathy, joint contracture, ophthalmoplegia syndrome
Illum syndrome
Intellectual disability, developmental delay, contracture syndrome
Intellectual disability, developmental delay, contracture syndrome
Kuskokwim syndrome
Larsen-like syndrome B3GAT3 type
Lethal congenital contracture syndrome type 1
Lethal congenital contracture syndrome type 2
Lethal congenital contracture syndrome type 3
Lethal congenital contracture syndrome type 5
Malignant hyperthermia with arthrogryposis and torticollis syndrome
Morse Rawnsley Sargent syndrome
NEK9-related lethal skeletal dysplasia
Neurogenic arthrogryposis multiplex congenita1
Prenatal-onset spinal muscular atrophy with congenital bone fractures
Van den Ende-Gupta syndrome
X-linked distal arthrogryposis multiplex congenita
X-linked lethal multiple pterygium syndrome