G23.0
BillableHallervorden-Spatz disease
Hallervorden-Spatz disease
Coding Notes
Inclusion Terms
Alternative clinical terms for this condition
- Pigmentary pallidal degeneration
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)
- multi-system degeneration of the autonomic nervous system (G90.3)
Also Known As / Clinical Terms
SNOMED CT
- Hallervorden-Spatz disease2992000
- Pigmentary pallidal atrophy2992000
- Pigmentary pallidal degeneration2992000
- Pallidal degeneration230302004
- Chorea due to heredodegenerative disorder722966004
- Dementia due to genetic disease1259476008
- Chorea due to classical neurodegeneration with brain iron accumulation type 11259611004
- Chorea due to classical pantothenate kinase associated neurodegeneration1259611004
- Chorea due to classical pigmentary pallidal degeneration1259611004
- Dementia due to atypical pantothenate kinase associated neurodegeneration1259679007
- Dementia due to atypical pigmentary pallidal degeneration1259679007
- Dementia due to neurodegeneration with brain iron accumulation type 11259679007
- Dementia due to classical neurodegeneration with brain iron accumulation type 11259990004
- Dementia due to classical pantothenate kinase associated neurodegeneration1259990004
- Dementia due to classical pigmentary pallidal degeneration1259990004
- Dystonia due to atypical pantothenate kinase associated neurodegeneration1260360005
- Dystonia due to atypical pigmentary pallidal degeneration1260360005
- Dystonia in neurodegeneration with brain iron accumulation type 11260360005
UMLS
- Brain Iron Accumulation Type I SyndromeC0018523
- Degeneration, Pigmentary PallidalC0018523
- Dystrophies, Juvenile-Onset NeuroaxonalC0018523
- Dystrophy, Juvenile-Onset NeuroaxonalC0018523
- HALLERVORDEN SPATZ DISC0018523
- HALLERVORDEN-SPATZ DISEASEC0018523
- HARP SYNDROME, FORMERLYC0018523
- HARP, FORMERLYC0018523
- HYPOPREBETALIPOPROTEINEMIA, ACANTHOCYTOSIS, RETINITIS PIGMENTOSA, AND PALLIDAL DEGENERATION, FORMERLYC0018523
- Hallervorden Spatz DiseaseC0018523
- Hallervorden Spatz SyndromeC0018523
- Hallervorden-Spatz DiseaseC0018523
- Hallervorden-Spatz SyndromeC0018523
- Hallervorden-Spatz diseaseC0018523
- Juvenile-Onset Neuroaxonal DystrophiesC0018523
- Juvenile-Onset Neuroaxonal DystrophyC0018523
- NBIA 1C0018523
- NBIA1C0018523
- NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 1C0018523
- Neuroaxonal Dystrophies, Juvenile-OnsetC0018523
- Neuroaxonal Dystrophy, Juvenile OnsetC0018523
- Neuroaxonal Dystrophy, Juvenile-OnsetC0018523
- Neurodegeneration With Brain Iron Accumulation 1C0018523
- Neurodegeneration with Brain Iron Accumulation Type 1C0018523
- Neurodegeneration with brain iron accumulation type 1C0018523
- Neurodegeneration, Pantothenate Kinase-AssociatedC0018523
- PANTOTHENATE KINASE-ASSOCIATED NEURODEGENERATIONC0018523
- PKANC0018523
- PKAN NEUROAXONAL DYSTROPHY, JUVENILE-ONSETC0018523
- PKAN Neuroaxonal Dystrophy, Juvenile OnsetC0018523
- PKAN Neuroaxonal Dystrophy, Juvenile-OnsetC0018523
- Pallidal Atrophy, PigmentaryC0018523
- Pantothenate Kinase Associated NeurodegenerationC0018523
- Pantothenate Kinase-Associated NeurodegenerationC0018523
- Pantothenate kinase-associated neurodegenerationC0018523
- Pigmentary Pallidal AtrophyC0018523
- Pigmentary Pallidal DegenerationC0018523
- Pigmentary pallidal atrophyC0018523
- Pigmentary pallidal degenerationC0018523
- Pigmentary pallidal degeneration (disorder)C0018523
- hallervorden spatz diseaseC0018523
- hallervorden spatz syndromeC0018523
- hallervorden-spatz diseaseC0018523
- hallervorden-spatz syndromeC0018523
Frequently Asked Questions
What is ICD-10 code G23.0?
ICD-10-CM code G23.0 represents "Hallervorden-Spatz disease". It is a billable/specific code that can be used on a claim.
Is G23.0 a billable code?
Yes, G23.0 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.
What chapter is G23.0 in?
G23.0 is in Chapter 6: Diseases of the Nervous System (codes G00-G99).
What SNOMED CT codes does G23.0 map to?
G23.0 maps to 8 SNOMED CT concepts: 1259611004, 722966004, 1259679007, 1259990004, 1259476008, and 3 more. SNOMED CT is a clinical terminology used in electronic health records.
What are the UMLS CUIs for G23.0?
G23.0 is linked to 1 UMLS Concept Unique Identifier: C0018523. 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.