Q74.3
BillableArthrogryposis multiplex congenita
Arthrogryposis multiplex congenita
Status
Billable / Specific
Parent Code
Q74Coding Notes
Also Known As / Clinical Terms
SNOMED CT
- Inherited disorder of bilirubin metabolism5655007
- Congenital hypoplasia of breast8915006
- Hypoplasia of breast8915006
- Hypoplastic breast8915006
- Congenital webbing of neck11731003
- Neck webbing11731003
- Webbed neck11731003
- Distal arthrogryposis24269006
- Distal arthrogryposis syndrome24269006
- Inherited arthrogryposis28204005
- Akinesia33994004
- HRF - Hepatorenal failure51292008
- Hepatorenal failure51292008
- Hepatorenal syndrome51292008
- Minicore disease55133004
- Multi-core congenital myopathy55133004
- Multi-core disease55133004
- Multi-minicore disease55133004
- Multicore disease55133004
- Multiminicore disease55133004
- Familial arthrogryposis - cholestatic hepatorenal syndrome62216007
- Familial arthrogryposis-cholestatic hepatorenal syndrome62216007
- Lethal familial cholestatic AND pigmentary liver disease62216007
- Anterior horn cell disease85672005
- Arthrogryposis111246005
- AMC - arthrogryposis multiplex congenita205402004
- Arthrogryposis multiplex congenita205402004
- Multiple congenital arthrogryposis205402004
- Congenital muscular dystrophy with arthrogryposis multiplex congenita240061000
- Hypoplasia of nipple268290005
- Rudimentary nipple268290005
- Congenital arthrogryposis caused by teratogen370473000
- MH - malignant hyperpyrexia405501007
- MHS - malignant hyperthermia susceptibility405501007
- Malignant hyperthermia405501007
- Hyperpyrexia409702008
- Arthrogryposis-like syndrome702447002
- Kuskokwim syndrome702447002
- Distal arthrogryposis type 2B715216008
- Freeman-Sheldon syndrome variant715216008
- Sheldon-Hall syndrome715216008
- Arthrogryposis with oculomotor limitation and electroretinal anomaly715217004
- Distal arthrogryposis type 5715217004
- Distal arthrogryposis with ophthalmoplegia715217004
- Oculomelic amyoplasia715217004
- Digitotalar dysmorphism715314008
- Distal arthrogryposis type 1715314008
- Neurogenic arthrogryposis multiplex congenita715316005
- Herva disease715418007
- Lethal congenital contracture syndrome type 1715418007
- Multiple contracture syndrome Finnish type715418007
- Lethal congenital contracture syndrome type 2715419004
- Multiple contracture syndrome Israeli-Bedouin type715419004
- Lethal congenital contracture syndrome type 3715420005
- Lethal arthrogryposis co-occurrent with anterior horn cell disease715565004
- Lethal arthrogryposis with anterior horn cell disease715565004
- Vuopala disease715565004
- Arthrogryposis with severe scoliosis715575001
- Distal arthrogryposis type 4715575001
- Camptodactyly with joint contracture and facial skeletal defect syndrome715986009
- Rozin Hertz Goodman syndrome715986009
- Rozin camptodactyly syndrome715986009
- Holoprosencephaly sequence with hypokinesia and congenital joint contracture syndrome716169009
- Morse Rawnsley Sargent syndrome716169009
- Froster Iskenius Waterson syndrome719398004
- Malignant hyperthermia with arthrogryposis and torticollis syndrome719398004
- Infantile-onset X-linked spinal muscular atrophy719836007
- Spinal muscular atrophy with arthrogryposis719836007
- X-linked distal arthrogryposis multiplex congenita719836007
- X-linked spinal muscular atrophy type 2719836007
- Adducted thumbs and arthrogryposis syndrome Christian type720463009
- ARC (arthrogryposis, renal dysfunction, cholestasis) syndrome720513002
- Arthrogryposis with renal dysfunction and cholestasis syndrome720513002
- Arthrogryposis multiplex congenita and whistling face syndrome720514008
- Illum syndrome720514008
- Arthrogryposis-like hand anomaly and sensorineural deafness syndrome720515009
- Distal arthrogryposis type 6720515009
- Arthrogryposis hyperkeratosis syndrome lethal form726620005
- Johnston Aarons Schelley syndrome726620005
- Autism spectrum disorder, epilepsy, arthrogryposis syndrome733623005
- SLC35A3-CDG - solute carrier family 35 member A3 congenital disorder of glycosylation733623005
- Fetal akinesia, cerebral and retinal haemorrhage syndrome763346009
- Fetal akinesia, cerebral and retinal hemorrhage syndrome763346009
- Foetal akinesia, cerebral and retinal haemorrhage syndrome763346009
- Lethal congenital contracture syndrome type 5763346009
- Autosomal recessive myogenic arthrogryposis multiplex congenita764812008
- SYNE1 (spectrin repeat containing nuclear envelope protein 1) related arthrogryposis multiplex congenita764812008
- SYNE1-related arthrogryposis multiplex congenita764812008
- Hypomyelination neuropathy arthrogryposis syndrome766931003
- DA5D - distal arthrogryposis type 5D773396009
- Distal arthrogryposis type 5 without ophthalmoparesis773396009
- Distal arthrogryposis type 5 without ophthalmoplegia773396009
- Distal arthrogryposis type 5D773396009
- Contractures, webbed neck, micrognathia, hypoplastic nipples syndrome773626008
- Dinno syndrome773626008
- Joint contracture, webbed neck, micrognathia, hypoplastic nipple syndrome773626008
- Pelvic dysplasia, arthrogryposis of lower limbs syndrome783140003
- Ray Peterson Scott syndrome783140003
- Arthrogryposis and ectodermal dysplasia syndrome786039009
- Arthrogryposis, ectodermal dysplasia, other anomalies syndrome786039009
- Stoll Alembik Finck syndrome786039009
- Camptodactyly, cleft palate, clubfoot syndrome897570002
- Distal arthrogryposis type 3897570002
- Distal arthrogryposis type IIA897570002
- Gordon syndrome897570002
- Congenital flexion contracture of foot joint1004071000
- X-linked distal hereditary motor neuropathy1156840002
- Congenital plantar flexion contracture1208482007
- DA10 - distal arthrogryposis type 101208482007
- Distal arthrogryposis type 101208482007
- MYBPC1-related autosomal recessive non-lethal arthrogryposis multiplex congenita syndrome1251451005
- Myosin binding protein C1-related autosomal recessive non-lethal arthrogryposis multiplex congenita syndrome1251451005
- Antenatal multi-minicore disease with arthrogryposis multiplex congenita1259119003
UMLS
- Arthrogryposis Multiplex Congenitas (AMC)C5779613
- Arthrogryposis multiplexC5779613
- AMC - arthrogryposis multiplex congenitaC5779613
- AMYOPLASIA CONGENC5779613
- ARTHROMYODYSPLASIA CONGENC5779613
- Amyoplasia CongenitaC5779613
- ArthrogryposesC5779613
- Arthrogryposes, Congenital MultipleC5779613
- ArthrogryposisC5779613
- Arthrogryposis Multiplex CongenitaC5779613
- Arthrogryposis Multiplex Congenita (AMC)C5779613
- Arthrogryposis Multiplex CongenitasC5779613
- Arthrogryposis multiplex congenitaC5779613
- Arthrogryposis multiplex congenita (AMC)C5779613
- Arthrogryposis multiplex congenita (disorder)C5779613
- Arthrogryposis, Congenital MultipleC5779613
- Arthrogryposis, congenitalC5779613
- Arthromyodysplasia, CongenitalC5779613
- Arthromyodysplasias, CongenitalC5779613
- CONGEN ARTHROMYODYSPLASIAC5779613
- Congenita, Arthrogryposis MultiplexC5779613
- Congenita, Arthrogryposis Multiplex (AMC)C5779613
- Congenital ArthromyodysplasiaC5779613
- Congenital ArthromyodysplasiasC5779613
- Congenital Multiple ArthrogryposesC5779613
- Congenital Multiple ArthrogryposisC5779613
- Congenital contractures, multipleC5779613
- Congenital multiplex arthrogryposisC5779613
- Congenitas, Arthrogryposis MultiplexC5779613
- Congenitas, Arthrogryposis Multiplex (AMC)C5779613
- Fibrous Ankylosis of Multiple JointsC5779613
- Guerin Stern SyndromeC5779613
- Guerin Stern syndromeC5779613
- Guerin-Stern SyndromeC5779613
- Guérin Stern SyndromeC5779613
- Guérin-Stern SyndromeC5779613
- Multiple Arthrogryposes, CongenitalC5779613
- Multiple Arthrogryposis, CongenitalC5779613
- Multiple congenital arthrogryposisC5779613
- Multiple congenital contracturesC5779613
- Multiplex Congenita, ArthrogryposisC5779613
- Multiplex Congenita, Arthrogryposis (AMC)C5779613
- Multiplex Congenitas, ArthrogryposisC5779613
- Multiplex Congenitas, Arthrogryposis (AMC)C5779613
- Myodystrophia Fetalis DeformansC5779613
- Otto SyndromeC5779613
- Rocher Sheldon SyndromeC5779613
- Rocher-Sheldon SyndromeC5779613
- Rossi SyndromeC5779613
- Syndrome, Guerin-SternC5779613
- Syndrome, Guérin-SternC5779613
- Syndrome, OttoC5779613
- Syndrome, Rocher-SheldonC5779613
- Syndrome, RossiC5779613
- arthrogryposesC5779613
- arthrogryposisC5779613
- multiple congenital contractureC5779613
- myodystrophia fetalis deformansC5779613
- syndrome ottoC5779613
Frequently Asked Questions
What is the ICD-10 code for arthrogryposis multiplex congenita?
The ICD-10-CM code for arthrogryposis multiplex congenita is Q74.3. The full clinical description is "Arthrogryposis multiplex congenita". Q74.3 is a billable/specific code that can be used on insurance claims and medical billing.
What does ICD-10 code Q74.3 mean?
ICD-10-CM code Q74.3 represents "Arthrogryposis multiplex congenita". It is classified under Chapter 17: Congenital Malformations, Deformations and Chromosomal Abnormalities and is a billable/specific code that can be used on a claim.
Is Q74.3 a billable code?
Yes, Q74.3 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.
What chapter is Q74.3 in?
Q74.3 is in Chapter 17: Congenital Malformations, Deformations and Chromosomal Abnormalities (codes Q00-Q99).
What codes cannot be used with Q74.3?
Q74.3 has Excludes1 notes indicating codes that cannot be used together with it, including: polydactyly (Q69.-); reduction defect of limb (Q71-Q73); syndactyly (Q70.-).
What SNOMED CT codes does Q74.3 map to?
Q74.3 maps to 50 SNOMED CT concepts: 205402004, 720513002, 720463009, 33994004, 1259119003, and 45 more. SNOMED CT is a clinical terminology used in electronic health records.
What are the UMLS CUIs for Q74.3?
Q74.3 is linked to 1 UMLS Concept Unique Identifier: C5779613. The UMLS (Unified Medical Language System) integrates multiple biomedical vocabularies maintained by the U.S. National Library of Medicine.
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Includes SNOMED Clinical Terms® (SNOMED CT®) used by permission of SNOMED International. Includes content from the UMLS Metathesaurus, courtesy of the U.S. National Library of Medicine.