ICD-10-CM Code G23.0
Billable CodeBillable codes are sufficient justification for admission to an acute care hospital when used a principal diagnosis.
G23.0 is a billable ICD code used to specify a diagnosis of hallervorden-Spatz disease. A 'billable code' is detailed enough to be used to specify a medical diagnosis.
The ICD code G230 is used to code Neuroferritinopathy
Neuroferritinopathy or adult-onset basal ganglia disease is a genetic neurodegenerative disorder characterized by the accumulation of iron in the basal ganglia, cerebellum, and motor cortex of the human brain. Symptoms, which are extrapyramidal in nature, progress slowly and generally do not become apparent until adulthood. These symptoms include chorea, dystonia, and cognitive deficits which worsen with age.
Coding Notes for G23.0 Info for medical coders on how to properly use this ICD-10 code
Inclusion TermsInclusion Terms are a list of concepts for which a specific code is used. The list of Inclusion Terms is useful for determining the correct code in some cases, but the list is not necessarily exhaustive.
- Pigmentary pallidal degeneration
- DRG Group #056-057 - Degenerative nervous system disorders with MCC.
- DRG Group #056-057 - Degenerative nervous system disorders without MCC.
ICD-10-CM Alphabetical Index References for 'G23.0 - Hallervorden-Spatz disease'
The ICD-10-CM Alphabetical Index links the below-listed medical terms to the ICD code G23.0. Click on any term below to browse the alphabetical index.
Equivalent ICD-9 Code GENERAL EQUIVALENCE MAPPINGS (GEM)
This is the official approximate match mapping between ICD9 and ICD10, as provided by the General Equivalency mapping crosswalk. This means that while there is no exact mapping between this ICD10 code G23.0 and a single ICD9 code, 333.0 is an approximate match for comparison and conversion purposes.
Parent Code: G23 - Other degenerative diseases of basal ganglia