Kodex

Code

G12.1

Other inherited spinal muscular atrophy

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Hierarchy

G00-G99 Diseases of the nervous system (G00-G99)
- G10-G14 Systemic atrophies primarily affecting the central nervous system (G10-G14)
  - G12 Spinal muscular atrophy and related syndromes
    - G12.0 Infantile spinal muscular atrophy, type I [Werdnig-Hoffman]
    - G12.1 Other inherited spinal muscular atrophy
    - G12.2 Motor neuron disease
    - G12.8 Other spinal muscular atrophies and related syndromes
    - G12.9 Spinal muscular atrophy, unspecified

Inclusion Terms

G12.1

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

Excludes 2

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