ICD-10-CM 2027
ICD-10 code for Kugelberg-Welander disease
From the official ICD-10-CM alphabetic index entry “Kugelberg-Welander disease”. Page updated September 29, 2026.
About coding Kugelberg-Welander disease
The ICD-10-CM code for Kugelberg-Welander disease is G12.1 (Other inherited spinal muscular atrophy).
Within G12, choose G12.1 (Other inherited spinal muscular atrophy) only when documentation doesn't support a more specific option: infantile spinal muscular atrophy, type I [Werdnig-Hoffman] (G12.0), motor neuron disease (G12.2), other spinal muscular atrophies and related syndromes (G12.8) and spinal muscular atrophy, unspecified (G12.9).
As a secondary diagnosis it is a CC (complication or comorbidity), which can move an inpatient stay into the "with CC" MS-DRG of its family, unless the principal diagnosis excludes it.
In MS-DRG v44.0, it is part of the grouping logic for DRG 056 (Degenerative Nervous System Disorders with MCC, relative weight 2.2655) and DRG 057 (Degenerative Nervous System Disorders without MCC, relative weight 1.2838), in MDC 01 (Diseases and Disorders of the Nervous System), as a principal or secondary diagnosis. The DRG a claim lands in depends on the principal diagnosis, procedures and any CC/MCC secondary diagnoses.
Common questions about Kugelberg-Welander disease ICD-10 codes
What is the ICD-10 code for Kugelberg-Welander disease?
- G12.1 — Other inherited spinal muscular atrophy.
Is G12.1 billable?
- Yes. G12.1 is a billable/specific ICD-10-CM code valid for FY2027 (October 1, 2026 – September 30, 2027).
Can G12.1 be used as a principal diagnosis?
- Yes. The Medicare Code Editor doesn't restrict G12.1 as a principal diagnosis.
Is G12.1 a CC or MCC?
- G12.1 is a CC (complication or comorbidity) under MS-DRG v44.0, unless excluded by the principal diagnosis.