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 period (P04-P96)
- certain infectious and parasitic diseases (A00-B99)
- complications of pregnancy, childbirth and the puerperium (O00-O9A)
- congenital malformations, deformations, and chromosomal abnormalities (Q00-Q99)
- endocrine, nutritional and metabolic diseases (E00-E88)
- injury, poisoning and certain other consequences of external causes (S00-T88)
- neoplasms (C00-D49)
- symptoms, signs and abnormal clinical and laboratory findings, not elsewhere classified (R00-R94)
- arthrogryposis multiplex congenita (Q74.3)
- metabolic disorders (E70-E88)
- myositis (M60.-)
Also Known As / Clinical Terms
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
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.
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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.