Progressive supranuclear ophthalmoplegia [Steele-Richardson-Olszewski]
Billable / specificHCC V28 199
G23.1 is a billable, specific ICD-10-CM code that can be used to indicate a diagnosis for reimbursement purposes in FY2027.
Inclusion terms
Applicable to
- Progressive supranuclear palsy
Excludes2
Not included here — may be reported together when both conditions exist.
- certain conditions originating in the perinatal period (P04-P96) (from G23)
- certain infectious and parasitic diseases (A00-B99) (from G23)
- complications of pregnancy, childbirth and the puerperium (O00-O9A) (from G23)
- congenital malformations, deformations, and chromosomal abnormalities (Q00-Q99) (from G23)
- endocrine, nutritional and metabolic diseases (E00-E88) (from G23)
- injury, poisoning and certain other consequences of external causes (S00-T88) (from G23)
- neoplasms (C00-D49) (from G23)
- symptoms, signs and abnormal clinical and laboratory findings, not elsewhere classified (R00-R94) (from G23)
- multi-system degeneration of the autonomic nervous system (G90.3) (from G23)
Also known as
- Progressive supranuclear palsy
- Ophthalmoplegia, supranuclear, progressive
- Palsy, bulbar, supranuclear
- Palsy, progressive supranuclear
- Paralysis, paralytic, progressive, supranuclear
- Paralysis, paralytic, supranuclear
- Steele-Richardson-Olszewski disease or syndrome
- Willige-Hunt disease or syndrome
Parent code
- G23Other degenerative diseases of basal gangliaHeader