2007 ICD-9-CM Volume 1 Diagnosis Codes Home > Diseases Of The Nervous System And Sense Organs 320-389 > Hereditary And Degenerative Diseases Of The Central Nervous System 330-338 > Anterior Horn Cell Disease 335.* >
 2007 ICD-9-CM Diagnosis 335.10
Spinal muscular atrophy unspecified On October 1, 2008 the 2009 ICD-9-CM codes came into effect. Therefore, this code may be out of date.
The 2009 version of ICD-9-CM 335.10 can be accessed here. - A group of disorders marked by progressive degeneration of motor neurons in the spinal cord resulting in weakness and muscular atrophy, usually without evidence of injury to the corticospinal tracts. Diseases in this category include Werdnig-Hoffmann disease and later onset SPINAL MUSCULAR ATROPHIES OF CHILDHOOD, most of which are hereditary. (Adams et al., Principles of Neurology, 6th ed, p1089)
- 335.10 is a specific code that can be used to specify a diagnosis
- 335.10 contains 7 index entries
- View the ICD-9-CM Volume 1 335.* hierarchy
Index entries containing 335.10:- Atrophy, atrophic
- muscle, muscular 728.2
- myelopathic (progressive)
 335.10
- progressive (familial) (hereditary) (pure) 335.21
- spinal 335.10
- spinal (progressive) 335.10
- spinal (cord) 336.8
- muscular (chronic) 335.10
- paralysis 335.10
- acute (see also Poliomyelitis, with paralysis) 045.1
Paralysis, paralytic (complete) (incomplete) 344.9- spinal (cord) NEC 344.1
- progressive 335.10
|
|
|
