G72.3
Periodic paralysis
This code does not map to a risk-adjusting HCC in the loaded models.
Coding notes
Excludes 1 never coded together · Excludes 2 may co-exist
paramyotonia congenita (of von Eulenburg) (G71.19)
Familial periodic paralysis Hyperkalemic periodic paralysis (familial) Hypokalemic periodic paralysis (familial) Myotonic periodic paralysis (familial) Normokalemic paralysis (familial) Potassium sensitive periodic paralysis
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)
Official Guidelines for G72.3
FY 2026 ›Find G72.3 in the alphabetic index
11 index paths lead to this code
- Adynamia
- Cavare's disease
- Gamstorp's disease
- Disease, diseased › Cavare's
- Disease, diseased › familial periodic paralysis
- Disease, diseased › Gamstorp's
- Paralysis, paralytic › familial
- Paralysis, paralytic › hyperkalemic periodic
- Paralysis, paralytic › hypokalemic periodic
- Paralysis, paralytic › normokalemic periodic
- Paralysis, paralytic › periodic