G71.9
BillablePrimary disorder of muscle, unspecified
Primary disorder of muscle, unspecified
Coding Notes
Inclusion Terms
Alternative clinical terms for this condition
- Hereditary myopathy NOS
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
- Hereditary myopathy associated with hydrocephalus53387004
- Proximal myopathy193255007
- Chronic deafness232325008
- Hereditary sclerosing poikiloderma238834002
- Weary-Kindler syndrome238834002
- Myopathy with cytoplasmic inclusions240086009
- Tendon contracture274141009
- Edstrom myopathy702373006
- HMERF - hereditary myopathy with early respiratory failure702373006
- Hereditary myopathy with early respiratory failure702373006
- Hereditary proximal myopathy with early respiratory failure702373006
- MPRM - myopathy, proximal, with early respiratory muscle involvement702373006
- Vacuolar myopathy719815005
- X-linked myopathy with excessive autophagy719815005
- Hereditary fibrosing poikiloderma, tendon contractures, myopathy, pulmonary fibrosis syndrome771306007
- POIKTMP (poikiloderma, tendon contractures, myopathy, pulmonary fibrosis) syndrome771306007
- POIKTMP syndrome771306007
- Peripheral neuropathy, myopathy, hoarseness, deafness syndrome782752005
- Peripheral neuropathy, myopathy, hoarseness, hearing loss syndrome782752005
- Autosomal dominant distal hereditary motor neuropathy1156837002
Frequently Asked Questions
What is ICD-10 code G71.9?
ICD-10-CM code G71.9 represents "Primary disorder of muscle, unspecified". It is a billable/specific code that can be used on a claim.
Is G71.9 a billable code?
Yes, G71.9 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.
What chapter is G71.9 in?
G71.9 is in Chapter 6: Diseases of the Nervous System (codes G00-G99).
What SNOMED CT codes does G71.9 map to?
G71.9 maps to 11 SNOMED CT concepts: 1156837002, 232325008, 702373006, 771306007, 53387004, and 6 more. SNOMED CT is a clinical terminology used in electronic health records.
What are the UMLS CUIs for G71.9?
G71.9 is linked to 2 UMLS Concept Unique Identifiers: C1399469, C0494503. 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.