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Inherited arthrogryposis 28204005 SNOMED CT code SNOMED code 28204005 name Inherited arthrogryposis status active date introduced 2002-01-31 fully specified name(s) Inherited arthrogryposis (disorder) synonyms Inherited arthrogryposis attributes - group1 Occurrence Congenital 255399007 Pathological process Pathological developmental process 308490002 Finding site Structure of joint region 785818007 Associated morphology Contracture 57048009 attributes - group2 Has interpretation Decreased 1250004 Interprets Range of joint movement 364564000 parents children Aase Smith type 1 syndrome 718576001 Adducted thumbs and arthrogryposis syndrome Christian type 720463009 Arthrogryposis and ectodermal dysplasia syndrome 786039009 Autism spectrum disorder, epilepsy, arthrogryposis syndrome 733623005 Autosomal dominant multiple pterygium syndrome 771269000 Autosomal recessive myogenic arthrogryposis multiplex congenita 764812008 Camptobrachydactyly 733045005 Congenital contractural arachnodactyly 205821003 Congenital lethal myopathy Compton North type 773306002 Congenital muscular dystrophy with arthrogryposis multiplex congenita 240061000 Contracture with ectodermal dysplasia and orofacial cleft syndrome 720746006 Digitotalar dysmorphism 715314008 Distal arthrogryposis type 10 1208482007 Distal arthrogryposis type 3 897570002 Distal arthrogryposis type 5D 773396009 Ehlers-Danlos syndrome musculocontractural type 720860004 Familial arthrogryposis-cholestatic hepatorenal syndrome 62216007 German syndrome 733037000 Hecht syndrome 8757006 Hereditary inclusion body myopathy, joint contracture, ophthalmoplegia syndrome 724349009 Hypomyelination neuropathy arthrogryposis syndrome 766931003 Illum syndrome 720514008 Intellectual disability, developmental delay, contracture syndrome 722456001 Kuskokwim syndrome 702447002 Larsen-like syndrome B3GAT3 type 763778003 Lethal arthrogryposis with anterior horn cell disease 715565004 Lethal congenital contracture syndrome type 1 715418007 Lethal congenital contracture syndrome type 2 715419004 Lethal congenital contracture syndrome type 3 715420005 Lethal congenital contracture syndrome type 5 763346009 Malignant hyperthermia with arthrogryposis and torticollis syndrome 719398004 Marden Walker syndrome 449824004 Morse Rawnsley Sargent syndrome 716169009 MYBPC1-related autosomal recessive non-lethal arthrogryposis multiplex congenita syndrome 1251451005 NEK9-related lethal skeletal dysplasia 1179299005 Neurogenic arthrogryposis multiplex congenita 715316005 Pena-Shokeir syndrome type I 401138005 Prenatal-onset spinal muscular atrophy with congenital bone fractures 1172689007 Van den Ende-Gupta syndrome 719845008 X-linked distal arthrogryposis multiplex congenita 719836007 X-linked lethal multiple pterygium syndrome 763462004 hierarchies a selection of possible paths
SNOMED CT Concept 138875005 404684003 417893002 276655000 111246005 28204005 138875005 404684003 64572001 5294002 363070008 28204005 ancestors sorted most to least specific
cpt crosswalks Rules-based maps relating CPT® codes to and from SNOMED CT® clinical concepts. Forward and backward mapping allows for easy transition between code sets. Map-A-Code crosswalk tool easily crosswalks multiple codes between the code sets.
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