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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 2007 ICD-9-CM Diagnosis 335.0 Werdnig-hoffmann disease This code may be outdated. View the most recent version of ICD-9-CM 335.0 335.0 is a specific code that can be used to specify a diagnosis 335.0 contains 9 index entries View the ICD-9-CM Volume 1 335.* hierarchy 335.0 also known as: Infantile spinal muscular atrophy Progressive muscular atrophy of infancy Index entries containing 335.0: Atrophy, atrophic muscle, muscular 728.2 infantile spinal 335.0 progressive (familial) (hereditary) (pure) 335.21 infantile (spinal) 335.0 spinal 335.10 infantile 335.0 spinal (progressive) 335.10 infantile 335.0 Werdnig-Hoffmann 335.0 Disease, diseased - see also Syndrome Werdnig-Hoffmann 335.0 Syndrome - see also Disease Hoffmann-Werdnig 335.0 Werdnig-Hoffmann 335.0 Werdnig-Hoffmann syndrome (muscular atrophy) 335.0