| Enrollment Model Type | Coeff Tag | Year | Weight Score |
|---|---|---|---|
| CFA | HCC190 |
2026 | + 1.427 |
| CFD | HCC190 |
2026 | + 3.642 |
| CNA | HCC190 |
2026 | + 1.175 |
| CND | HCC190 |
2026 | + 1.792 |
| CPA | HCC190 |
2026 | + 0.640 |
| CPD | HCC190 |
2026 | + 1.243 |
| INS | HCC190 |
2026 | + 0.628 |
The following diagnoses map directly to HCC 190 under the V28 risk adjustment model:
| ICD-10 Code | Clinical Diagnosis Description | Guideline |
|---|---|---|
| G12.0 | Infantile spinal muscular atrophy, type I [Werdnig-Hoffman] | Notes ↗ |
| G12.1 | Other inherited spinal muscular atrophy | Notes ↗ |
| G12.20 | Motor neuron disease, unspecified | Notes ↗ |
| G12.21 | Amyotrophic lateral sclerosis | Notes ↗ |
| G12.22 | Progressive bulbar palsy | Notes ↗ |
| G12.23 | Primary lateral sclerosis | Notes ↗ |
| G12.24 | Familial motor neuron disease | Notes ↗ |
| G12.25 | Progressive spinal muscle atrophy | Notes ↗ |
| G12.29 | Other motor neuron disease | Notes ↗ |
| G12.8 | Other spinal muscular atrophies and related syndromes | Notes ↗ |
| G12.9 | Spinal muscular atrophy, unspecified | Notes ↗ |