Oculomelic amyoplasia
Arthrogryposis hyperkeratosis syndrome lethal form
Multiplex Congenitas, Arthrogryposis (AMC)
Congenital muscular dystrophy with arthrogryposis multiplex congenita
Multiple Arthrogryposis, Congenital
Lethal congenital contracture syndrome type 3
Inherited disorder of bilirubin metabolism
Antenatal multi-minicore disease with arthrogryposis multiplex congenita
Minicore disease
Pelvic dysplasia, arthrogryposis of lower limbs syndrome
X-linked distal arthrogryposis multiplex congenita
Arthrogryposis with renal dysfunction and cholestasis syndrome
Johnston Aarons Schelley syndrome
Distal arthrogryposis type 6
MH - malignant hyperpyrexia
Malignant hyperthermia
Adducted thumbs and arthrogryposis syndrome Christian type
Arthrogryposes
Hyperpyrexia
AMC - arthrogryposis multiplex congenita
Arthrogryposis multiplex congenita (disorder)
AMYOPLASIA CONGEN
SYNE1-related arthrogryposis multiplex congenita
Arthrogryposis, ectodermal dysplasia, other anomalies syndrome
Familial arthrogryposis-cholestatic hepatorenal syndrome
Congenita, Arthrogryposis Multiplex
Distal arthrogryposis type 10
Fetal akinesia, cerebral and retinal hemorrhage syndrome
Akinesia
MYBPC1-related autosomal recessive non-lethal arthrogryposis multiplex congenita syndrome
Multi-core disease
Multiplex Congenita, Arthrogryposis (AMC)
Rozin camptodactyly syndrome
Autism spectrum disorder, epilepsy, arthrogryposis syndrome
Lethal arthrogryposis co-occurrent with anterior horn cell disease
Distal arthrogryposis type 5 without ophthalmoparesis
Dinno syndrome
Guérin Stern Syndrome
Freeman-Sheldon syndrome variant
Congenital webbing of neck
Infantile-onset X-linked spinal muscular atrophy
Neck webbing
Congenital multiplex arthrogryposis
Autosomal recessive myogenic arthrogryposis multiplex congenita
Distal arthrogryposis
Hypomyelination neuropathy arthrogryposis syndrome
Camptodactyly with joint contracture and facial skeletal defect syndrome
Congenital flexion contracture of foot joint
Arthrogryposis Multiplex Congenitas
Myosin binding protein C1-related autosomal recessive non-lethal arthrogryposis multiplex congenita syndrome
Multi-minicore disease
Congenitas, Arthrogryposis Multiplex
Multiminicore disease
Arthrogryposis with severe scoliosis
Congenital Multiple Arthrogryposis
Distal arthrogryposis syndrome
Congenital plantar flexion contracture
Hypoplasia of nipple
Arthrogryposis
Ray Peterson Scott syndrome
Arthrogryposis, congenital
Holoprosencephaly sequence with hypokinesia and congenital joint contracture syndrome
Anterior horn cell disease
Camptodactyly, cleft palate, clubfoot syndrome
Multiplex Congenitas, Arthrogryposis
Multiple contracture syndrome Finnish type
Congenital Arthromyodysplasia
Herva disease
multiple congenital contracture
Hypoplasia of breast
Rozin Hertz Goodman syndrome
Arthrogryposis Multiplex Congenita (AMC)
Congenital Multiple Arthrogryposes
Multiple Arthrogryposes, Congenital
Congenitas, Arthrogryposis Multiplex (AMC)
SYNE1 (spectrin repeat containing nuclear envelope protein 1) related arthrogryposis multiplex congenita
Multiple contracture syndrome Israeli-Bedouin type
Hepatorenal failure
Foetal akinesia, cerebral and retinal haemorrhage syndrome
Distal arthrogryposis type 5
Hypoplastic breast
Rossi Syndrome
Lethal congenital contracture syndrome type 2
Distal arthrogryposis type 3
Neurogenic arthrogryposis multiplex congenita
Malignant hyperthermia with arthrogryposis and torticollis syndrome
Lethal congenital contracture syndrome type 1
HRF - Hepatorenal failure
myodystrophia fetalis deformans
Kuskokwim syndrome
DA5D - distal arthrogryposis type 5D
Digitotalar dysmorphism
Arthrogryposis with oculomotor limitation and electroretinal anomaly
Arthrogryposis and ectodermal dysplasia syndrome
Gordon syndrome
Spinal muscular atrophy with arthrogryposis
Distal arthrogryposis type 5D
Syndrome, Rossi
Multiplex Congenita, Arthrogryposis
Syndrome, Rocher-Sheldon
ARTHROMYODYSPLASIA CONGEN
Arthrogryposis-like syndrome
Syndrome, Guerin-Stern
Rudimentary nipple
Multiple congenital arthrogryposis
Familial arthrogryposis - cholestatic hepatorenal syndrome
Lethal familial cholestatic AND pigmentary liver disease
Congenital Arthromyodysplasias
MHS - malignant hyperthermia susceptibility
Fetal akinesia, cerebral and retinal haemorrhage syndrome
Joint contracture, webbed neck, micrognathia, hypoplastic nipple syndrome
Arthrogryposis multiplex
Guerin Stern Syndrome
Syndrome, Otto
syndrome otto
Congenita, Arthrogryposis Multiplex (AMC)
Froster Iskenius Waterson syndrome
Congenital arthrogryposis caused by teratogen
Vuopala disease
Distal arthrogryposis type 4
Guerin-Stern Syndrome
X-linked spinal muscular atrophy type 2
Arthrogryposis Multiplex Congenitas (AMC)
Distal arthrogryposis type 2B
Syndrome, Guérin-Stern
Arthromyodysplasias, Congenital
Arthrogryposis, Congenital Multiple
Stoll Alembik Finck syndrome
CONGEN ARTHROMYODYSPLASIA
Webbed neck
Guérin-Stern Syndrome
Lethal arthrogryposis with anterior horn cell disease
Amyoplasia Congenita
Sheldon-Hall syndrome
Contractures, webbed neck, micrognathia, hypoplastic nipples syndrome
Distal arthrogryposis type IIA
X-linked distal hereditary motor neuropathy
Distal arthrogryposis type 1
Arthrogryposes, Congenital Multiple
Fibrous Ankylosis of Multiple Joints
ARC (arthrogryposis, renal dysfunction, cholestasis) syndrome
Inherited arthrogryposis
Morse Rawnsley Sargent syndrome
Distal arthrogryposis type 5 without ophthalmoplegia
Arthrogryposis multiplex congenita and whistling face syndrome
SLC35A3-CDG - solute carrier family 35 member A3 congenital disorder of glycosylation
Arthrogryposis-like hand anomaly and sensorineural deafness syndrome
Distal arthrogryposis with ophthalmoplegia
Rocher-Sheldon Syndrome
Otto Syndrome
Congenital contractures, multiple
Multicore disease
Arthromyodysplasia, Congenital
Rocher Sheldon Syndrome
Illum syndrome
Multi-core congenital myopathy
Lethal congenital contracture syndrome type 5
DA10 - distal arthrogryposis type 10
Hepatorenal syndrome
Congenital hypoplasia of breast
Multiple congenital contractures

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.

How does Q74.3 relate to ICF functioning codes?

ICF (International Classification of Functioning, Disability and Health) codes describe how conditions like arthrogryposis multiplex congenita affect a person's functioning — body functions, activities, participation, and environmental factors. AutoICD provides ICF Core Sets for 12+ conditions and can map clinical text to ICF categories automatically. Browse the ICF directory to explore functioning codes.

What is the ICD-11 equivalent of Q74.3?

Q74.3 maps to the ICD-11 code: LD26.41 (Arthrogryposis multiplex congenita).

Automate ICD-10 Coding With AI

Send clinical text to the AutoICD API and get back structured ICD-10 codes with confidence scores. Integrates into any EHR or billing system in minutes.

Try Free View API Docs

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.