G72.3
BillablePeriodic paralysis
Periodic paralysis
Coding Notes
Inclusion Terms
Alternative clinical terms for this condition
- Familial periodic paralysis
- Hyperkalemic periodic paralysis (familial)
- Hypokalemic periodic paralysis (familial)
- Myotonic periodic paralysis (familial)
- Normokalemic paralysis (familial)
- Potassium sensitive periodic paralysis
Excludes 1
Codes that cannot be used together with this code (mutual exclusion)
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)
Also Known As / Clinical Terms
SNOMED CT
- Secondary periodic paralysis7409003
- Hashitoxic periodic paralysis30967002
- Thyrotoxic periodic paralysis30967002
- Familial normokalaemic periodic paralysis40381009
- Familial normokalemic periodic paralysis40381009
- Normokalaemic periodic paralysis40381009
- Normokalemic periodic paralysis40381009
- Periodic paralysis III40381009
- Sodium-responsive periodic paralysis40381009
- Familial hypokalaemic periodic paralysis82732003
- Familial hypokalemic periodic paralysis82732003
- HOKPP - hypokalaemic periodic paralysis82732003
- HOKPP - hypokalemic periodic paralysis82732003
- Hypokalaemic periodic paralysis82732003
- Hypokalemic periodic paralysis82732003
- Periodic paralysis I82732003
- Periodic paralysis198030008
- Cavarre disease267607008
- Familial myoplegia267607008
- Familial periodic paralysis267607008
- Familial recurrent paralysis267607008
- Myoplegic dystrophy267607008
- Periodic myotonia267607008
- Adynamia episodica hereditaria304737009
- Familial hyperkalaemic periodic paralysis304737009
- Familial hyperkalemic periodic paralysis304737009
- Gamstorp disease304737009
- Hyperkalaemic periodic paralysis304737009
- Hyperkalemic periodic paralysis304737009
- Periodic paralysis II304737009
- Periodic paralysis with transient compartment-like syndrome774153002
- Periodic paralysis with later-onset distal motor neuropathy774154008
UMLS
- ADYNAMIA EPISODICA HEREDITARIA WITH OR WITHOUT MYOTONIAC0238357
- Adynamia Episodica HereditariaC0238357
- Adynamia Episodica Hereditaria with or without MyotoniaC0238357
- Adynamia episodica hereditariaC0238357
- Disease, GamstorpC0238357
- Familial Hyperkalemic Periodic ParalysisC0238357
- Familial hyperkalaemic periodic paralysisC0238357
- Familial hyperkalemic periodic paralysisC0238357
- Familial hyperkalemic periodic paralysis (disorder)C0238357
- GAMSTORP DISEASEC0238357
- Gamstorp DiseaseC0238357
- Gamstorp Episodic AdynamyC0238357
- Gamstorp diseaseC0238357
- Gamstorp episodic adynamyC0238357
- HYPERKALEMIC PERIODIC PARALYSISC0238357
- HYPPC0238357
- HyperKPPC0238357
- HyperPPC0238357
- Hyperkalaemic periodic paralysisC0238357
- Hyperkalemic Periodic ParalysisC0238357
- Hyperkalemic Periodic Paralysis, FamilialC0238357
- Hyperkalemic periodic paralysisC0238357
- Hyperkalemic periodic paralysis (familial)C0238357
- Myotonic Periodic ParalysisC0238357
- Paralysis, Hyperkalemic PeriodicC0238357
- Paralysis, Periodic, Hyperkalemic, FamilialC0238357
- Periodic hyperkalemic paralysisC0238357
- Periodic paralysis IIC0238357
- Primary Hyperkalemic Periodic ParalysisC0238357
- Primary hyperkalemic periodic paralysisC0238357
- Sodium Channel Muscle DiseaseC0238357
- adynamia episodica hereditariaC0238357
- hyperkalaemic periodic paralysisC0238357
- hyperkalemic paralysis periodicC0238357
- hyperkalemic periodic paralysisC0238357
- periodic paralysis hyperkalemicC0238357
- periodic paralysis iiC0238357
- Cavarre diseaseC0030443
- Familial Periodic ParalysesC0030443
- Familial Periodic ParalysisC0030443
- Familial myoplegiaC0030443
- Familial periodic paralysisC0030443
- Familial periodic paralysis (disorder)C0030443
- Familial recurrent paralysisC0030443
- Myoplegic dystrophyC0030443
- Paralyses, Familial PeriodicC0030443
- Paralysis periodicC0030443
- Paralysis, Familial PeriodicC0030443
- Periodic Paralyses, FamilialC0030443
- Periodic Paralysis, FamilialC0030443
- Periodic myotoniaC0030443
- familial paralysis periodicC0030443
- familial periodic paralysisC0030443
- paralysis periodicC0030443
- periodic familial paralysisC0030443
- periodic paralysisC0030443
- periodic paralysis familialC0030443
- Episodic paralysisC1279412
- Periodic paralysisC1279412
- Periodic paralysis (finding)C1279412
- Familial Hypokalemic Periodic ParalysisC0238358
- Familial hypokalaemic periodic paralysisC0238358
- Familial hypokalemic periodic paralysisC0238358
- Familial hypokalemic periodic paralysis (disorder)C0238358
- HOKPPC0238358
- HOKPP - hypokalaemic periodic paralysisC0238358
- HOKPP - hypokalemic periodic paralysisC0238358
- HYPOKPPC0238358
- HYPOPPC0238358
- HypoKPPC0238358
- HypoPPC0238358
- Hypokalaemic periodic paralysisC0238358
- Hypokalemic Periodic ParalysisC0238358
- Hypokalemic Periodic Paralysis, FamilialC0238358
- Hypokalemic periodic paralysisC0238358
- Hypokalemic periodic paralysis (familial)C0238358
- Paralysis, Hypokalemic PeriodicC0238358
- Periodic Paralysis HypokalemicC0238358
- Periodic Paralysis, HypokalemicC0238358
- Periodic Paralysis- HypokalemicC0238358
- Periodic Paralysis- HypokalemicsC0238358
- Periodic paralysis IC0238358
- Primary Hypokalemic Periodic ParalysisC0238358
- Primary hypokalemic periodic paralysisC0238358
- Westphall DiseaseC0238358
- Westphall diseaseC0238358
- hypokalaemic paralysis periodicC0238358
- hypokalaemic periodic paralysisC0238358
- hypokalemic paralysis periodicC0238358
- hypokalemic periodic paralysisC0238358
- periodic hypokalaemic paralysisC0238358
- periodic hypokalemic paralysisC0238358
- Myotonic periodic paralysis (familial)C2875318
- Normokalemic paralysis (familial)C2875319
- Potassium sensitive periodic paralysisC1955768
Frequently Asked Questions
What is ICD-10 code G72.3?
ICD-10-CM code G72.3 represents "Periodic paralysis". It is a billable/specific code that can be used on a claim.
Is G72.3 a billable code?
Yes, G72.3 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.
What chapter is G72.3 in?
G72.3 is in Chapter 6: Diseases of the Nervous System (codes G00-G99).
What codes cannot be used with G72.3?
G72.3 has Excludes1 notes indicating codes that cannot be used together with it, including: arthrogryposis multiplex congenita (Q74.3); dermatopolymyositis (M33.-); ischemic infarction of muscle (M62.2-); and 3 more.
What SNOMED CT codes does G72.3 map to?
G72.3 maps to 9 SNOMED CT concepts: 304737009, 267607008, 82732003, 40381009, 30967002, and 4 more. SNOMED CT is a clinical terminology used in electronic health records.
What are the UMLS CUIs for G72.3?
G72.3 is linked to 7 UMLS Concept Unique Identifiers: C0238357, C0030443, C1279412, C0238358, C2875318, and 2 more. 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.