| Source | Code | Name | Case count | Share of cases (%) |
|---|---|---|---|---|
| OUTPAT | OUTPAT_ICD10(G122) | Motor neuron disease | 726 | |
| INPAT | INPAT_ICD10(G122) | Motor neuron disease | 592 | |
| DEATH | DEATH_ICD10(G122) | Motor neuron disease | 487 | |
| PRIM_OUT | PRIM_OUT_NOT_USED_ICD10(G122) | Motor neuron disease. Not used in endpoint definition. POSSIBLY INACCURATE IN COMPLEX ENDPOINTS! | 387 | |
| OUTPAT | OUTPAT_ICD10(G119) | Hereditary ataxia, unspecified | 194 | |
| OUTPAT | OUTPAT_ICD10(G129) | Spinal muscular atrophy, unspecified | 130 | |
| OUTPAT | OUTPAT_ICD10(G112) | Late-onset cerebellar ataxia | 121 | |
| OUTPAT | OUTPAT_ICD10(G128) | Other spinal muscular atrophies and related syndromes | 97 | |
| INPAT | INPAT_ICD10(G119) | Hereditary ataxia, unspecified | 96 | |
| OUTPAT | OUTPAT_ICD10(G118) | Other hereditary ataxias | 69 | |
| PRIM_OUT | PRIM_OUT_NOT_USED_ICD10(G112) | Late-onset cerebellar ataxia. Not used in endpoint definition. POSSIBLY INACCURATE IN COMPLEX ENDPOINTS! | 63 | |
| OUTPAT | OUTPAT_ICD10(G121) | Other inherited spinal muscular atrophy | 57 | |
| OUTPAT | OUTPAT_ICD10(G114) | Hereditary spastic paraplegia | 48 | |
| PRIM_OUT | PRIM_OUT_NOT_USED_ICD10(G119) | Hereditary ataxia, unspecified. Not used in endpoint definition. POSSIBLY INACCURATE IN COMPLEX ENDPOINTS! | 45 | |
| INPAT | INPAT_ICD10(G129) | Spinal muscular atrophy, unspecified | 44 | |
| PRIM_OUT | PRIM_OUT_NOT_USED_ICD10(G129) | Spinal muscular atrophy, unspecified. Not used in endpoint definition. POSSIBLY INACCURATE IN COMPLEX ENDPOINTS! | 43 | |
| OUTPAT | OUTPAT_ICD10(G10) | Huntington's disease | 39 | |
| INPAT | INPAT_ICD10(G112) | Late-onset cerebellar ataxia | 37 | |
| PRIM_OUT | PRIM_OUT_NOT_USED_ICD10(G118) | Other hereditary ataxias. Not used in endpoint definition. POSSIBLY INACCURATE IN COMPLEX ENDPOINTS! | 37 | |
| PRIM_OUT | PRIM_OUT_NOT_USED_ICD10(G128) | Other spinal muscular atrophies and related syndromes. Not used in endpoint definition. POSSIBLY INACCURATE IN COMPLEX ENDPOINTS! | 37 | |
| INPAT | INPAT_ICD10(G128) | Other spinal muscular atrophies and related syndromes | 34 | |
| PRIM_OUT | PRIM_OUT_NOT_USED_ICD10(G121) | Other inherited spinal muscular atrophy. Not used in endpoint definition. POSSIBLY INACCURATE IN COMPLEX ENDPOINTS! | 33 | |
| INPAT | INPAT_ICD10(G118) | Other hereditary ataxias | 32 | |
| INPAT | INPAT_ICD10(G121) | Other inherited spinal muscular atrophy | 31 | |
| PRIM_OUT | PRIM_OUT_NOT_USED_ICD10(G114) | Hereditary spastic paraplegia. Not used in endpoint definition. POSSIBLY INACCURATE IN COMPLEX ENDPOINTS! | 29 | |
| INPAT | INPAT_ICD10(G114) | Hereditary spastic paraplegia | 26 | |
| INPAT | INPAT_ICD10(G10) | Huntington's disease | 24 | |
| OUTPAT | OUTPAT_ICD10(G130) | Paraneoplastic neuromyopathy and neuropathy | 19 | |
| PRIM_OUT | PRIM_OUT_NOT_USED_ICD10(G10) | Huntington's disease. Not used in endpoint definition. POSSIBLY INACCURATE IN COMPLEX ENDPOINTS! | 18 | |
| PRIM_OUT | PRIM_OUT_NOT_USED_ICD10(G1102) | Dysequilibrium syndrome. Not used in endpoint definition. POSSIBLY INACCURATE IN COMPLEX ENDPOINTS! | 17 | |
| OUTPAT | OUTPAT_ICD10(G1118) | Early-onset cerebellar ataxia | 15 | |
| OUTPAT | OUTPAT_ICD10(G120) | Infantile spinal muscular atrophy, type I [Werdnig-Hoffman] | 14 | |
| INPAT | INPAT_ICD10(G130) | Paraneoplastic neuromyopathy and neuropathy | 12 | |
| OUTPAT | OUTPAT_ICD10(G1100) | Cerebellar dysplasia and aplasia | 12 | |
| PRIM_OUT | PRIM_OUT_NOT_USED_ICD10(G1118) | Early-onset cerebellar ataxia. Not used in endpoint definition. POSSIBLY INACCURATE IN COMPLEX ENDPOINTS! | 11 | |
| INPAT | INPAT_ICD10(G1118) | Early-onset cerebellar ataxia | 10 | |
| PRIM_OUT | PRIM_OUT_NOT_USED_ICD10(G11) | Hereditary ataxia. Not used in endpoint definition. POSSIBLY INACCURATE IN COMPLEX ENDPOINTS! | 10 | |
| PRIM_OUT | PRIM_OUT_NOT_USED_ICD10(G130) | Paraneoplastic neuromyopathy and neuropathy. Not used in endpoint definition. POSSIBLY INACCURATE IN COMPLEX ENDPOINTS! | 10 | |
| OUTPAT | OUTPAT_ICD10(G1102) | Dysequilibrium syndrome | 9 | |
| OUTPAT | OUTPAT_ICD10(G132) | Systemic atrophy primarily affecting central nervous system in myxoedema (E00.1, E03) | 8 | |
| DEATH | DEATH_ICD10(G10) | Huntington's disease | 6 | |
| DEATH | DEATH_ICD10(G112) | Late-onset cerebellar ataxia | 6 | |
| DEATH | DEATH_ICD10(G118) | Other hereditary ataxias | 6 | |
| DEATH | DEATH_ICD10(G129) | Spinal muscular atrophy, unspecified | 6 | |
| INPAT | INPAT_ICD10(G120) | Infantile spinal muscular atrophy, type I [Werdnig-Hoffman] | 6 | |
| INPAT | INPAT_ICD10(G131) | Other systemic atrophy primarily affecting central nervous system in neoplastic disease | 5 | |
| PRIM_OUT | PRIM_OUT_NOT_USED_ICD10(G12) | Spinal muscular atrophy and related syndromes. Not used in endpoint definition. POSSIBLY INACCURATE IN COMPLEX ENDPOINTS! | 5 |