Striatonigral degeneration
ICD-10 Code
G23.2
Striatonigral degeneration
Definition
A progressive neurodegenerative disorder caused by a disruption in the connection between the striatum and the substantia nigra. It is a type of multiple system atrophy (MSA). Signs and symptoms include rigidity, instability, impaired speech, and slow movements.
Also identified as
- DOID 4751 per MONDO
- ICD10CM G23.2 per MONDO
- ICD9 333.0 per MONDO
- MESH D020955 per MONDO
- NCIT C125695 per MONDO
- SCTID 29618004 per MONDO
- UMLS C0270733 per MONDO
Affected Organs
| Organ | Involvement | Source |
|---|---|---|
| Central nervous system | Disease Has Associated Anatomic Site | NCIT · CC BY 4.0 |
| Central nervous system | Disease Has Primary Anatomic Site | NCIT · CC BY 4.0 |
| Nervous system | Disease Has Associated Anatomic Site | NCIT · CC BY 4.0 |
| Nervous system | Disease Has Primary Anatomic Site | NCIT · CC BY 4.0 |