G71.8
BillableOther primary disorders of muscles
Other primary disorders of muscles
Coding Notes
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
- Atrophy of tongue50805004
- Tongue atrophy50805004
- Tongue wasting50805004
- Wasting of tongue50805004
- Familial visceral myopathy63684002
- Hereditary hollow viscus myopathy63684002
- Proximal myopathy193255007
- Benign monomelic amyotrophy230256009
- Amyotrophy caused by herpes zoster230262004
- Chronic intestinal pseudo-obstruction235828008
- Hollow visceral myopathy235831009
- X-linked muscular dystrophy with limb girdle distribution240047005
- X-linked limb girdle muscular dystrophy with normal dystrophin240051007
- Hereditary myopathy limited to females240053005
- Myopathy with cytoplasmic inclusions240086009
- Myopathy due to calsequestrin and SERCA1 (sarcoplasmic/endoplasmic reticulum calcium ATPase 1) protein overload724095006
- Myopathy due to calsequestrin and SERCA1 protein overload724095006
- Myopathy due to calsequestrin and sarcoplasmic/endoplasmic reticulum calcium ATPase 1 protein overload724095006
- Proximal myopathy with extrapyramidal signs770722002
- Hereditary inclusion body myopathy type 4770786001
- X-linked myopathy with postural muscle atrophy773729007
- XMPMA - X-linked myopathy with postural muscle atrophy773729007
- Fatal infantile hypertonic myofibrillar myopathy782883004
- Alpha-B crystallin-related late-onset distal myopathy783770002
- Alpha-B crystallin-related late-onset myopathy783770002
- Late-onset distal crystallinopathy783770002
- Childhood-onset autosomal recessive myopathy with external ophthalmoplegia787172004
- Autosomal dominant distal hereditary motor neuropathy1156837002
- Kyphosis, lateral tongue atrophy, myofibrillar myopathy syndrome1172591008
- Autosomal dominant distal axonal motor neuropathy, myofibrillar myopathy syndrome1179294000
- Benign monomelic amyotrophy of lower limb1263539004
- Monomelic amyotrophy of lower limb1263539004
- Benign monomelic amyotrophy of upper limb1263540002
- Monomelic amyotrophy of upper limb1263540002
Frequently Asked Questions
What is the ICD-10 code for other primary disorders of muscles?
The ICD-10-CM code for other primary disorders of muscles is G71.8. The full clinical description is "Other primary disorders of muscles". G71.8 is a billable/specific code that can be used on insurance claims and medical billing.
What does ICD-10 code G71.8 mean?
ICD-10-CM code G71.8 represents "Other primary disorders of muscles". 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 G71.8 a billable code?
Yes, G71.8 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.
What chapter is G71.8 in?
G71.8 is in Chapter 6: Diseases of the Nervous System (codes G00-G99).
What SNOMED CT codes does G71.8 map to?
G71.8 maps to 23 SNOMED CT concepts: 783770002, 230262004, 50805004, 1179294000, 1156837002, and 18 more. SNOMED CT is a clinical terminology used in electronic health records.
What are the UMLS CUIs for G71.8?
G71.8 is linked to 1 UMLS Concept Unique Identifier: C0477404. 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.