Diagnosis Code: Q74.3

Short Description: Arthrogryposis multiplex congenita

Long Description: Arthrogryposis multiplex congenita

The code Q74.3 is VALID for claim submission

Code Classification:

• Congenital malformations, deformations and chromosomal abnormalities (Q00-Q99)
  • Congenital malformations and deformations of the musculoskeletal system (Q65-Q79)
    • Other congenital malformations of limb(s) (Q74)
      • Q74.3 Arthrogryposis multiplex congenita

Code Version: 2022 ICD-10-CM

Synonyms

• Adducted thumbs and arthrogryposis syndrome Christian type
• Akinesia
• Akinesia
• Akinesia
• Antenatal multi-minicore disease with arthrogryposis multiplex congenita
• Anterior horn cell disease
• Arthrogryposis
• Arthrogryposis and ectodermal dysplasia syndrome
• Arthrogryposis hyperkeratosis syndrome lethal form
• Arthrogryposis with oculomotor limitation and electroretinal anomaly
• Arthrogryposis with renal dysfunction and cholestasis syndrome
• Autism spectrum disorder, epilepsy, arthrogryposis syndrome
• Autosomal recessive myogenic arthrogryposis multiplex congenita
• Congenital abnormality of nipple
• Congenital arthrogryposis due to teratogen
• Congenital hypoplasia of breast
• Congenital muscular dystrophy with arthrogryposis multiplex congenita
• Digitotalar dysmorphism
• Distal arthrogryposis syndrome
• Distal arthrogryposis type 10
• Distal arthrogryposis type 3
• Distal arthrogryposis type 4
• Distal arthrogryposis type 5D
• Distal arthrogryposis type 6
• Familial arthrogryposis-cholestatic hepatorenal syndrome
• Hepatorenal syndrome
• Hyperpyrexia
• Hypomyelination neuropathy arthrogryposis syndrome
• Hypoplasia of nipple
• Illum syndrome
• Inherited arthrogryposis
• Inherited disorder of bilirubin metabolism
• Inherited disorder of bilirubin metabolism
• Joint contracture, webbed neck, micrognathia, hypoplastic nipple syndrome
• Kuskokwim syndrome
• Lethal arthrogryposis with anterior horn cell disease
• 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
• Malignant hyperthermia with arthrogryposis and torticollis syndrome
• Morse Rawnsley Sargent syndrome
• Multi-core congenital myopathy
• MYBPC1-related autosomal recessive non-lethal arthrogryposis multiplex congenita syndrome
• Neck webbing
• Neurogenic arthrogryposis multiplex congenita
• Neurogenic arthrogryposis multiplex congenita
• Pelvic dysplasia, arthrogryposis of lower limbs syndrome
• Rozin Hertz Goodman syndrome
• Sheldon-Hall syndrome
• X-linked distal arthrogryposis multiplex congenita
• X-linked distal hereditary motor neuropathy

Diagnostic Related Group(s)

The code Q74.3 is grouped in the following Diagnostic Related Group(s) (MS-DRG v39.0)

• Other Musculoskeletal System And Connective Tissue Diagnoses With Mcc (564)
• Other Musculoskeletal System And Connective Tissue Diagnoses With Cc (565)
• Other Musculoskeletal System And Connective Tissue Diagnoses Without Cc/mcc (566)

Crosswalk Information

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This page was last updated on: 10/1/2023

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