Degenerative disease of the spinal cord
334
Neurological
Both
330-337.99, 341-349.99
ICD mappings
| ICD code | Type | Description | Phenome |
|---|---|---|---|
| G11 | ICD10CM | Hereditary ataxia | MGI |
| G11.0 | ICD10CM | Congenital nonprogressive ataxia | MGI |
| G11.1 | ICD10CM | Early-onset cerebellar ataxia | MGI |
| G11.2 | ICD10CM | Late-onset cerebellar ataxia | MGI |
| G11.3 | ICD10CM | Cerebellar ataxia with defective DNA repair | MGI |
| G11.4 | ICD10CM | Hereditary spastic paraplegia | MGI |
| G11.8 | ICD10CM | Other hereditary ataxias | MGI |
| G11.9 | ICD10CM | Hereditary ataxia, unspecified | MGI |
| G12.0 | ICD10CM | Infantile spinal muscular atrophy, type I [Werdnig-Hoffman] | MGI |
| G12.1 | ICD10CM | Other inherited spinal muscular atrophy | MGI |
| G12.2 | ICD10CM | Motor neuron disease | MGI |
| G12.20 | ICD10CM | Motor neuron disease, unspecified | MGI |
| G12.21 | ICD10CM | Amyotrophic lateral sclerosis | MGI |
| G12.22 | ICD10CM | Progressive bulbar palsy | MGI |
| G12.23 | ICD10CM | Primary lateral sclerosis | MGI |
| G12.24 | ICD10CM | Familial motor neuron disease | MGI |
| G12.25 | ICD10CM | Progressive spinal muscle atrophy | MGI |
| G12.29 | ICD10CM | Other motor neuron disease | MGI |
| G12.8 | ICD10CM | Other spinal muscular atrophies and related syndromes | MGI |
| G12.9 | ICD10CM | Spinal muscular atrophy, unspecified | MGI |
| G32.0 | ICD10CM | Subacute combined degeneration of spinal cord in diseases classified elsewhere | MGI |
| G32.8 | ICD10CM | Other specified degenerative disorders of nervous system in diseases classified elsewhere | MGI |
| G32.81 | ICD10CM | Cerebellar ataxia in diseases classified elsewhere | MGI |
| G32.89 | ICD10CM | Other specified degenerative disorders of nervous system in diseases classified elsewhere | MGI |
| G95 | ICD10CM | Other and unspecified diseases of spinal cord | MGI |
| G95.0 | ICD10CM | Syringomyelia and syringobulbia | MGI |
| G95.1 | ICD10CM | Vascular myelopathies | MGI |
| G95.11 | ICD10CM | Acute infarction of spinal cord (embolic) (nonembolic) | MGI |
| G95.19 | ICD10CM | Other vascular myelopathies | MGI |
| G95.2 | ICD10CM | Other and unspecified cord compression | MGI |
| G95.20 | ICD10CM | Unspecified cord compression | MGI |
| G95.29 | ICD10CM | Other cord compression | MGI |
| G95.8 | ICD10CM | Other specified diseases of spinal cord | MGI |
| G95.81 | ICD10CM | Conus medullaris syndrome | MGI |
| G95.89 | ICD10CM | Other specified diseases of spinal cord | MGI |
| G95.9 | ICD10CM | Disease of spinal cord, unspecified | MGI |
| G99.2 | ICD10CM | Myelopathy in diseases classified elsewhere | MGI |
| 334.0 | ICD9CM | Friedreich's ataxia | MGI |
| 334.1 | ICD9CM | Hereditary spastic paraplegia | MGI |
| 334.2 | ICD9CM | Primary cerebellar degeneration | MGI |
| 334.3 | ICD9CM | Other cerebellar ataxia | MGI |
| 334.4 | ICD9CM | Cerebellar ataxia in diseases classified elsewhere | MGI |
| 334.8 | ICD9CM | Other spinocerebellar diseases | MGI |
| 334.9 | ICD9CM | Spinocerebellar disease, unspecified | MGI |
| 335.0 | ICD9CM | Werdnig-Hoffmann disease | MGI |
| 335.10 | ICD9CM | Spinal muscular atrophy, unspecified | MGI |
| 335.11 | ICD9CM | Kugelberg-Welander disease | MGI |
| 335.19 | ICD9CM | Other spinal muscular atrophy | MGI |
| 335.20 | ICD9CM | Amyotrophic lateral sclerosis | MGI |
| 335.21 | ICD9CM | Progressive muscular atrophy | MGI |
| 335.22 | ICD9CM | Progressive bulbar palsy | MGI |
| 335.23 | ICD9CM | Pseudobulbar palsy | MGI |
| 335.24 | ICD9CM | Primary lateral sclerosis | MGI |
| 335.29 | ICD9CM | Other motor neuron disease | MGI |
| 335.8 | ICD9CM | Other anterior horn cell diseases | MGI |
| 335.9 | ICD9CM | Anterior horn cell disease, unspecified | MGI |
| 336.0 | ICD9CM | Syringomyelia and syringobulbia | MGI |
| 336.1 | ICD9CM | Vascular myelopathies | MGI |
| 336.2 | ICD9CM | Subacute combined degeneration of spinal cord in diseases classified elsewhere | MGI |
| 336.3 | ICD9CM | Myelopathy in other diseases classified elsewhere | MGI |
| 336.8 | ICD9CM | Other myelopathy | MGI |
| 336.9 | ICD9CM | Unspecified disease of spinal cord | MGI |
| G11.0 | ICD10 | G11.0 Congenital nonprogressive ataxia | UKB |
| G11.1 | ICD10 | G11.1 Early-onset cerebellar ataxia | UKB |
| G11.2 | ICD10 | G11.2 Late-onset cerebellar ataxia | UKB |
| G11.3 | ICD10 | G11.3 Cerebellar ataxia with defective DNA repair | UKB |
| G11.4 | ICD10 | G11.4 Hereditary spastic paraplegia | UKB |
| G11.8 | ICD10 | G11.8 Other hereditary ataxias | UKB |
| G11.9 | ICD10 | G11.9 Hereditary ataxia, unspecified | UKB |
| G12.0 | ICD10 | G12.0 Infantile spinal muscular atrophy, type I [Werdnig-Hoffman] | UKB |
| G12.1 | ICD10 | G12.1 Other inherited spinal muscular atrophy | UKB |
| G12.2 | ICD10 | G12.2 Motor neuron disease | UKB |
| G12.8 | ICD10 | G12.8 Other spinal muscular atrophies and related syndromes | UKB |
| G12.9 | ICD10 | G12.9 Spinal muscular atrophy, unspecified | UKB |
| G32.0 | ICD10 | G32.0 Subacute combined degeneration of spinal cord in diseases classified elsewhere | UKB |
| G95.0 | ICD10 | G95.0 Syringomyelia and syringobulbia | UKB |
| G95.1 | ICD10 | G95.1 Vascular myelopathies | UKB |
| G95.2 | ICD10 | G95.2 Cord compression, unspecified | UKB |
| G95.8 | ICD10 | G95.8 Other specified diseases of spinal cord | UKB |
| G95.9 | ICD10 | G95.9 Disease of spinal cord, unspecified | UKB |
| G99.2 | ICD10 | G99.2 Myelopathy in diseases classified elsewhere | UKB |
| 336 | ICD9 | 336 Other diseases of spinal cord | UKB |
| 336.0 | ICD9 | 3360 Syringomyelia and syringobulbia | UKB |
| 336.1 | ICD9 | 3361 Vascular myelopathies | UKB |
| 336.2 | ICD9 | 3362 Subacute combined degeneration of spinal cord | UKB |
| 336.3 | ICD9 | 3363 Myelopathy in other diseases classified elsewhere | UKB |
| 336.8 | ICD9 | 3368 Other specified myelopathy | UKB |
| 336.9 | ICD9 | 3369 Unspecified diseases of the spinal cord | UKB |
This page is mainly a phenotype dictionary entry. When you are trying to find candidate PRS models, go to the Scores table, search by trait or exposure name, and then use the score-detail and PheWAS pages for model-specific follow-up.