335.0 - Werdnig-Hoffmann Disease
The ICD 9 Code for Werdnig-Hoffmann disease is listed as 335.0.
Additional information concerning this code and description can be found below including ICD 10 crosswalks / GEMS, and chapter information where available.
ICD 9 CM Field | Value |
---|---|
Diagnosis Code: | 335.0 |
Long Description: | Werdnig-Hoffmann disease |
Short Description: | Werdnig-hoffmann disease |
Chapter: | Diseases Of The Nervous System And Sense Organs |
Block: | Hereditary And Degenerative Diseases Of The Central Nervous System (330-337) |
ICD-10-CM Diagnosis Codes General Equivalence Mappings (GEMS): | |
ICD-10-CM Code: | G12.0 - Infantile spinal muscular atrophy, type I [Werdnig-Hoffman] |
ICD-9-CM Siblings (same level / similar specificity) of 335.0: | |
335.8 - Other anterior horn cell diseases | |
335.9 - Anterior horn cell disease, unspecified |