G71.13
BillableMyotonic chondrodystrophy
Myotonic chondrodystrophy
Coding Notes
Inclusion Terms
Alternative clinical terms for this condition
- Chondrodystrophic myotonia
- Congenital myotonic chondrodystrophy
- Schwartz-Jampel disease
Excludes 2
Conditions not included here, but the patient may have both
- •certain conditions originating in the perinatal periodP04-P96
- •certain infectious and parasitic diseasesA00-B99
- •complications of pregnancy, childbirth and the puerperiumO9A)O00
- •congenital malformations, deformations, and chromosomal abnormalitiesQ00-Q99
- •endocrine, nutritional and metabolic diseasesE00-E88
- •injury, poisoning and certain other consequences of external causesS00-T88
- •neoplasmsC00-D49
- •symptoms, signs and abnormal clinical and laboratory findings, not elsewhere classifiedR00-R94
- •arthrogryposis multiplex congenitaQ74.3
- •metabolic disordersE70-E88
- •myositisM60
Related Codes(4)
Also Known As / Clinical Terms(76)
SNOMED CT
- Aberfeld syndrome29145002
- Burton skeletal dysplasia29145002
- Burton syndrome29145002
- Catel Hempel syndrome29145002
- Chondrodystrophic myotonia29145002
- Myotonia chondrodystrophica29145002
- Osteochondromuscular dystrophy29145002
- Schwartz-Jampel syndrome29145002
- Congenital myotonia726051002
- Myotonia congenita726051002
UMLS
- Aberfeld syndromeC0036391
- Burton skeletal dysplasiaC0036391
- Burton syndromeC0036391
- CHONDRODYSTROPHIC MYOTONIAC0036391
- Catel Hempel syndromeC0036391
- Chondrodystrophic MyotoniaC0036391
- Chondrodystrophic myotoniaC0036391
- Chondrodystrophy, MyotonicC0036391
- Congenital myotonic chondrodystrophyC0036391
- MYOTONIC MYOPATHY, DWARFISM, CHONDRODYSTROPHY, AND OCULAR AND FACIAL ABNORMALITIESC0036391
- Myotonia chondrodystrophicaC0036391
- Myotonia, ChondrodystrophicC0036391
- Myotonic ChondrodystrophyC0036391
- Myotonic Myopathy, Dwarfism, Chondrodystrophy, And Ocular And Facial AbnormalitiesC0036391
- Myotonic chondrodystrophyC0036391
- Myotonic myopathy, dwarfism, chondrodystrophy, and ocular and facial abnormalitiesC0036391
- Osteochondromuscular dystrophyC0036391
- SCHWARTZ-JAMPEL SYNDROMEC0036391
- SCHWARTZ-JAMPEL-ABERFELD SYNDROMEC0036391
- SJA SYNDROMEC0036391
- SJA SyndromeC0036391
- SJA syndromeC0036391
- SJSC0036391
- SJS1C0036391
- Schwartz Jampel Aberfeld syndromeC0036391
- Schwartz Jampel SyndromeC0036391
- Schwartz Jampel syndromeC0036391
- Schwartz-Jampel SyndromeC0036391
- Schwartz-Jampel diseaseC0036391
- Schwartz-Jampel syndromeC0036391
- Schwartz-Jampel syndrome (disorder)C0036391
- Schwartz-Jampel-Aberfeld SyndromeC0036391
- Schwartz-Jampel-Aberfeld syndromeC0036391
- Spondylo-Epimetaphyseal Dysplasia With MyotoniaC0036391
- Syndrome, Schwartz-Jampel-AberfeldC0036391
- aberfeld syndromeC0036391
- jampel schwartz syndromeC0036391
- schwartz jampel syndromeC0036391
- schwartz syndromeC0036391
- schwartz-jampel syndromeC0036391
Clinical Terms
- Schwartz-Jampel syndrome (disorder)
- Myotonia congenita
- Schwartz Jampel syndrome
- Myotonia, Chondrodystrophic
- SCHWARTZ-JAMPEL SYNDROME
- Schwartz-Jampel-Aberfeld syndrome
- Burton skeletal dysplasia
- SJA SYNDROME
- Syndrome, Schwartz-Jampel-Aberfeld
- aberfeld syndrome
- Chondrodystrophic myotonia
- Congenital myotonia
- Congenital myotonic chondrodystrophy
- SJS1
- schwartz syndrome
- Chondrodystrophy, Myotonic
- Spondylo-Epimetaphyseal Dysplasia With Myotonia
- Osteochondromuscular dystrophy
- jampel schwartz syndrome
- Myotonic myopathy, dwarfism, chondrodystrophy, and ocular and facial abnormalities
- Schwartz Jampel Aberfeld syndrome
- Myotonia chondrodystrophica
- Burton syndrome
- Schwartz-Jampel disease
- Catel Hempel syndrome
- SJS
Frequently Asked Questions
What is the ICD-10 code for myotonic chondrodystrophy?
The ICD-10-CM code for myotonic chondrodystrophy is G71.13. The full clinical description is "Myotonic chondrodystrophy". G71.13 is a billable/specific code that can be used on insurance claims and medical billing.
What does ICD-10 code G71.13 mean?
ICD-10-CM code G71.13 represents “Myotonic chondrodystrophy”. It is classified under Chapter 6: Diseases of the Nervous System and is a billable/specific code that can be used on a claim.
Is G71.13 a billable code?
Yes, G71.13 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.
What chapter is G71.13 in?
G71.13 is in Chapter 6: Diseases of the Nervous System (codes G00-G99).
What SNOMED CT codes does G71.13 map to?
G71.13 maps to 2 SNOMED CT concepts: 29145002, 726051002. SNOMED CT is a clinical terminology used in electronic health records.
What are the UMLS CUIs for G71.13?
G71.13 is linked to 1 UMLS Concept Unique Identifier: C0036391. The UMLS (Unified Medical Language System) integrates multiple biomedical vocabularies maintained by the U.S. National Library of Medicine.
How does G71.13 relate to ICF functioning codes?
ICF (International Classification of Functioning, Disability and Health) codes describe how conditions like myotonic chondrodystrophy 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 G71.13?
There is no direct ICD-11 mapping available for G71.13 in the WHO crosswalk tables. This may mean the concept is classified differently in ICD-11. Use the ICD-10 to ICD-11 converter to search for related codes.
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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.