G25.82
BillableStiff-man syndrome
Stiff-man syndrome
Coding Notes
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)
- sleep related movement disorders (G47.6-)
Also Known As / Clinical Terms
SNOMED CT
UMLS
- Congenital Stiff Man SyndromeC0085292
- Congenital Stiff-Man SyndromeC0085292
- Congenital Stiff-Man SyndromesC0085292
- Congenital Stiff-Person SyndromeC0085292
- Congenital Stiff-Person SyndromesC0085292
- Congenital stiff-man syndromeC0085292
- Congenital stiff-person syndromeC0085292
- Gamma neuron overactivity syndromeC0085292
- Moersch Woltmann SyndromeC0085292
- Moersch-Woltman syndromeC0085292
- Moersch-Woltmann SyndromeC0085292
- SPSC0085292
- STIFF-MAN SYNDROMEC0085292
- STIFF-PERSON SYNDROMEC0085292
- STIFF-TRUNK SYNDROMEC0085292
- Startle SyndromeC0085292
- Startle SyndromesC0085292
- Startle syndromeC0085292
- Stiff Man SyndromeC0085292
- Stiff Person SyndromeC0085292
- Stiff Trunk SyndromeC0085292
- Stiff man syndromeC0085292
- Stiff person spectrum disorderC0085292
- Stiff person spectrum disorder (disorder)C0085292
- Stiff person syndromeC0085292
- Stiff-Baby SyndromeC0085292
- Stiff-Baby SyndromesC0085292
- Stiff-Man SyndromeC0085292
- Stiff-Man Syndrome, CongenitalC0085292
- Stiff-Man Syndromes, CongenitalC0085292
- Stiff-Person SyndromeC0085292
- Stiff-Person Syndrome, CongenitalC0085292
- Stiff-Person Syndromes, CongenitalC0085292
- Stiff-Trunk SyndromeC0085292
- Stiff-Trunk SyndromesC0085292
- Stiff-baby syndromeC0085292
- Stiff-man syndromeC0085292
- Stiff-person syndromeC0085292
- Stiffman SyndromeC0085292
- Syndrome, Congenital Stiff-ManC0085292
- Syndrome, Congenital Stiff-PersonC0085292
- Syndrome, Moersch-WoltmannC0085292
- Syndrome, StartleC0085292
- Syndrome, Stiff-BabyC0085292
- Syndrome, Stiff-ManC0085292
- Syndrome, Stiff-PersonC0085292
- Syndrome, Stiff-TrunkC0085292
- Syndrome, StiffmanC0085292
- Syndromes, Congenital Stiff-ManC0085292
- Syndromes, Congenital Stiff-PersonC0085292
- Syndromes, StartleC0085292
- Syndromes, Stiff-BabyC0085292
- Syndromes, Stiff-TrunkC0085292
- mans stiff syndromeC0085292
- moersch woltman syndromeC0085292
- moersch-woltman syndromeC0085292
- moersch-woltmann syndromeC0085292
- person stiff syndromeC0085292
- persons stiff syndromeC0085292
- stiff man syndromeC0085292
- stiff mans syndromeC0085292
- stiff person syndromeC0085292
- stiff-man syndromeC0085292
- stiff-person syndromeC0085292
- stiffman syndromeC0085292
Frequently Asked Questions
What is ICD-10 code G25.82?
ICD-10-CM code G25.82 represents "Stiff-man syndrome". It is a billable/specific code that can be used on a claim.
Is G25.82 a billable code?
Yes, G25.82 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.
What chapter is G25.82 in?
G25.82 is in Chapter 6: Diseases of the Nervous System (codes G00-G99).
What SNOMED CT codes does G25.82 map to?
G25.82 maps to 2 SNOMED CT concepts: 230651008, 5217008. SNOMED CT is a clinical terminology used in electronic health records.
What are the UMLS CUIs for G25.82?
G25.82 is linked to 1 UMLS Concept Unique Identifier: C0085292. 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.