G11.11
BillableFriedreich ataxia
Friedreich ataxia
Coding Notes
Inclusion Terms
Alternative clinical terms for this condition
- Autosomal recessive Friedreich ataxia
- Friedreich ataxia with retained reflexes
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)
- cerebral palsy (G80.-)
- hereditary and idiopathic neuropathy (G60.-)
- metabolic disorders (E70-E88)
Also Known As / Clinical Terms
SNOMED CT
- FA - Friedreich ataxia10394003
- FRDA - Friedreich ataxia10394003
- Familial ataxia10394003
- Friedreich ataxia10394003
- Friedreich's ataxia10394003
- Friedreich's disease10394003
- Dilated cardiomyopathy due to Friedreich ataxia50270004
- Dilated cardiomyopathy due to Friedreich's ataxia50270004
- Cerebellar ataxia associated with another disorder192874000
- Cardiomyopathy in Friedreich ataxia195030007
- Cardiomyopathy in Friedreich's ataxia195030007
- Hypertrophic cardiomyopathy due to Friedreich ataxia890119003
- Posterior cord syndrome due to Friedreich ataxia1343511009
UMLS
- Ataxia, FriedreichC0016719
- Ataxia, Friedreich FamilialC0016719
- Ataxia, Friedreich HereditaryC0016719
- Ataxia, Friedreich SpinocerebellarC0016719
- Ataxia, Friedreich'sC0016719
- Ataxia, Friedreich's FamilialC0016719
- Ataxia, Friedreich's HereditaryC0016719
- Ataxias, FriedreichC0016719
- Ataxias, Friedreich's HereditaryC0016719
- Disease, FriedreichC0016719
- Disease, Friedreich'sC0016719
- FA - Friedreich ataxiaC0016719
- FRDAC0016719
- FRDA - Friedreich ataxiaC0016719
- FRIEDREICH ATAXIAC0016719
- FRIEDREICH DISC0016719
- FRIEDREICHS DISC0016719
- Familial Ataxia, FriedreichC0016719
- Familial Ataxia, Friedreich'sC0016719
- Familial ataxiaC0016719
- Friedreich AtaxiaC0016719
- Friedreich AtaxiasC0016719
- Friedreich DiseaseC0016719
- Friedreich Familial AtaxiaC0016719
- Friedreich Hereditary AtaxiaC0016719
- Friedreich Hereditary Spinal AtaxiaC0016719
- Friedreich Spinocerebellar AtaxiaC0016719
- Friedreich ataxiaC0016719
- Friedreich ataxia (disorder)C0016719
- Friedreich spinocerebellar ataxiaC0016719
- Friedreich's AtaxiaC0016719
- Friedreich's DiseaseC0016719
- Friedreich's Familial AtaxiaC0016719
- Friedreich's Hereditary AtaxiaC0016719
- Friedreich's Hereditary AtaxiasC0016719
- Friedreich's Hereditary Spinal AtaxiaC0016719
- Friedreich's ataxiaC0016719
- Friedreich's diseaseC0016719
- Friedreich's tabesC0016719
- Friedreichs Familial AtaxiaC0016719
- Friedreichs Hereditary AtaxiaC0016719
- Friedrich's ataxiaC0016719
- Hereditary Ataxia, FriedreichC0016719
- Hereditary Ataxia, Friedreich'sC0016719
- Hereditary Ataxias, Friedreich'sC0016719
- Hereditary Spinal Ataxia, FriedreichC0016719
- Hereditary Spinal Ataxia, Friedreich'sC0016719
- Hereditary Spinal SclerosesC0016719
- Hereditary Spinal SclerosisC0016719
- Scleroses, Hereditary SpinalC0016719
- Sclerosis, Hereditary SpinalC0016719
- Spinal Scleroses, HereditaryC0016719
- Spinal Sclerosis, HereditaryC0016719
- Spinocerebellar Ataxia, FriedreichC0016719
- ataxia friedreichC0016719
- ataxia friedrich'sC0016719
- familial ataxiaC0016719
- family ataxiaC0016719
- friedreich ataxiaC0016719
- friedreich diseaseC0016719
- friedreich's ataxiaC0016719
- friedreich's diseaseC0016719
- friedreich's hereditary ataxiaC0016719
- friedreichs ataxiaC0016719
- friedrich's ataxiaC0016719
- friedrick's ataxiaC0016719
- spinal sclerosis hereditaryC0016719
- Autosomal recessive Friedreich ataxiaC2875045
- FARRC1847416
- FRIEDREICH ATAXIA WITH RETAINED REFLEXESC1847416
- Friedreich Ataxia with Retained ReflexesC1847416
- Friedreich ataxia with retained reflexesC1847416
Frequently Asked Questions
What is the ICD-10 code for friedreich ataxia?
The ICD-10-CM code for friedreich ataxia is G11.11. The full clinical description is "Friedreich ataxia". G11.11 is a billable/specific code that can be used on insurance claims and medical billing.
What does ICD-10 code G11.11 mean?
ICD-10-CM code G11.11 represents "Friedreich ataxia". 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 G11.11 a billable code?
Yes, G11.11 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.
What chapter is G11.11 in?
G11.11 is in Chapter 6: Diseases of the Nervous System (codes G00-G99).
What SNOMED CT codes does G11.11 map to?
G11.11 maps to 6 SNOMED CT concepts: 195030007, 192874000, 50270004, 10394003, 890119003, and 1 more. SNOMED CT is a clinical terminology used in electronic health records.
What are the UMLS CUIs for G11.11?
G11.11 is linked to 3 UMLS Concept Unique Identifiers: C0016719, C2875045, C1847416. 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.