G12.1

Other inherited spinal muscular atrophy

Billable / specificHCC V28 190

G12.1 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

  • Adult form spinal muscular atrophy
  • Childhood form, type II spinal muscular atrophy
  • Distal spinal muscular atrophy
  • Juvenile form, type III spinal muscular atrophy [Kugelberg-Welander]
  • Progressive bulbar palsy of childhood [Fazio-Londe]
  • Scapuloperoneal form spinal muscular atrophy

Excludes2

Not included here — may be reported together when both conditions exist.

  • certain conditions originating in the perinatal period (P04-P96) (from G12)
  • certain infectious and parasitic diseases (A00-B99) (from G12)
  • complications of pregnancy, childbirth and the puerperium (O00-O9A) (from G12)
  • congenital malformations, deformations, and chromosomal abnormalities (Q00-Q99) (from G12)
  • endocrine, nutritional and metabolic diseases (E00-E88) (from G12)
  • injury, poisoning and certain other consequences of external causes (S00-T88) (from G12)
  • neoplasms (C00-D49) (from G12)
  • symptoms, signs and abnormal clinical and laboratory findings, not elsewhere classified (R00-R94) (from G12)

Also known as

  • Adult form spinal muscular atrophy
  • Childhood form, type II spinal muscular atrophy
  • Distal spinal muscular atrophy
  • Juvenile form, type III spinal muscular atrophy [Kugelberg-Welander]
  • Progressive bulbar palsy of childhood [Fazio-Londe]
  • Scapuloperoneal form spinal muscular atrophy
  • Atrophy, atrophic, muscle, muscular, progressive, adult
  • Atrophy, atrophic, muscle, muscular, spinal, adult form
  • Atrophy, atrophic, muscle, muscular, spinal, childhood form, type II
  • Atrophy, atrophic, muscle, muscular, spinal, distal
  • Atrophy, atrophic, muscle, muscular, spinal, hereditary NEC
  • Atrophy, atrophic, muscle, muscular, spinal, juvenile form, type III
  • Atrophy, atrophic, muscle, muscular, spinal, scapuloperoneal form
  • Fazio-Londe disease or syndrome
  • Kugelberg-Welander disease
  • Palsy, bulbar, of childhood

Parent code

  • G12Spinal muscular atrophy and related syndromesHeader

Related codes

  • G12.0Infantile spinal muscular atrophy, type I [Werdnig-Hoffman]Billable
  • G12.2Motor neuron diseaseHeader
  • G12.8Other spinal muscular atrophies and related syndromesBillable
  • G12.9Spinal muscular atrophy, unspecifiedBillable

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