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ICD-10-CM Codes Browse (Tabular) Diagnostic External Drug Neoplasm

G12.0 – Infantile spinal muscular atrophy, type I [Werdnig-Hoffman]

Overview

Coding Notes

Active
Billable, valid for HIPAA-covered transactions

GEM Conversion to ICD-9 CM

Fs: 00000 – Werdnig-Hoffmann disease

MDC / MS-DRG Reference

DEGENERATIVE NERVOUS SYSTEM DISORDERS WITH MCC
DEGENERATIVE NERVOUS SYSTEM DISORDERS WITHOUT MCC

Back Reference of Diagnostic Codes

Atrophy, atrophic (of)
muscle, muscular (diffuse) (general) (idiopathic) (primary) M62.50
infantile spinal G12.0
progressive (bulbar) G12.21
infantile (spinal) G12.0
spinal G12.25
infantile G12.0
spinal G12.9
infantile, type I (Werdnig-Hoffmann) G12.0
Werdnig-Hoffmann G12.0
Disease, diseased See also Syndrome
Werdnig-Hoffmann G12.0
Syndrome See also Disease
Hoffmann-Werdnig G12.0
Werdnig-Hoffman G12.0
Werdnig-Hoffmann syndrome (muscular atrophy) G12.0

Sibling Codes

Other inherited spinal muscular atrophy
Motor neuron disease
Other spinal muscular atrophies and related syndromes
Spinal muscular atrophy, unspecified

Parent Sibling Codes

Huntington's disease
Hereditary ataxia
Spinal muscular atrophy and related syndromes
Systemic atrophies primarily affecting central nervous system in diseases classified elsewhere
Postpolio syndrome

View in Tabular

Code Title
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]