Inherited arthrogryposis

Inherited arthrogryposis (disorder)

active

Code	`28204005`
Semantic tag	disorder
Module	international
Definition	defined
Effective time	20020731

Parents (3)

111246005Arthrogryposis disorder
363070008Developmental hereditary disorder disorder
363212003Hereditary disorder of musculoskeletal system disorder

Children (44)

718576001Aase Smith type 1 syndrome disorder
720463009Adducted thumbs and arthrogryposis syndrome Christian type disorder
1351836007Alkuraya Kucinskas syndrome disorder
786039009Arthrogryposis and ectodermal dysplasia syndrome disorder
733623005Autism spectrum disorder, epilepsy, arthrogryposis syndrome disorder
771269000Autosomal dominant multiple pterygium syndrome disorder
764812008Autosomal recessive myogenic arthrogryposis multiplex congenita disorder
733045005Camptobrachydactyly disorder
205821003Congenital contractural arachnodactyly disorder
773306002Congenital lethal myopathy Compton North type disorder
240061000Congenital muscular dystrophy with arthrogryposis multiplex congenita disorder
1300190004Congenital pontocerebellar hypoplasia type 12 disorder
720746006Contracture with ectodermal dysplasia and orofacial cleft syndrome disorder
715314008Digitotalar dysmorphism disorder
1208482007Distal arthrogryposis type 10 disorder
897570002Distal arthrogryposis type 3 disorder
773396009Distal arthrogryposis type 5D disorder
720860004Ehlers-Danlos syndrome musculocontractural type disorder
62216007Familial arthrogryposis-cholestatic hepatorenal syndrome disorder
52616002Freeman-Sheldon syndrome disorder
733037000German syndrome disorder
8757006Hecht syndrome disorder
724349009Hereditary inclusion body myopathy, joint contracture, ophthalmoplegia syndrome disorder
766931003Hypomyelination neuropathy arthrogryposis syndrome disorder
720514008Illum syndrome disorder
722456001Intellectual disability, developmental delay, contracture syndrome disorder
702447002Kuskokwim syndrome disorder
763778003Larsen-like syndrome B3GAT3 type disorder
715565004Lethal arthrogryposis with anterior horn cell disease disorder
715418007Lethal congenital contracture syndrome type 1 disorder
715419004Lethal congenital contracture syndrome type 2 disorder
715420005Lethal congenital contracture syndrome type 3 disorder
763346009Lethal congenital contracture syndrome type 5 disorder
1251451005MYBPC1-related autosomal recessive non-lethal arthrogryposis multiplex congenita syndrome disorder
719398004Malignant hyperthermia with arthrogryposis and torticollis syndrome disorder
449824004Marden Walker syndrome disorder
716169009Morse Rawnsley Sargent syndrome disorder
1179299005NEK9-related lethal skeletal dysplasia disorder
715316005Neurogenic arthrogryposis multiplex congenita disorder
401138005Pena-Shokeir syndrome type I disorder
1172689007Prenatal-onset spinal muscular atrophy with congenital bone fractures disorder
719845008Van den Ende-Gupta syndrome disorder
719836007X-linked distal arthrogryposis multiplex congenita disorder
763462004X-linked lethal multiple pterygium syndrome disorder