Hereditary retinal dystrophies
362.7
Sense Organs
Both
250.70-250.79,360-365.99
ICD mappings
| ICD code | Type | Description | Phenome |
|---|---|---|---|
| H31.11 | ICD10CM | Age-related choroidal atrophy | MGI |
| H31.111 | ICD10CM | Age-related choroidal atrophy, right eye | MGI |
| H31.112 | ICD10CM | Age-related choroidal atrophy, left eye | MGI |
| H31.113 | ICD10CM | Age-related choroidal atrophy, bilateral | MGI |
| H31.119 | ICD10CM | Age-related choroidal atrophy, unspecified eye | MGI |
| H35.5 | ICD10CM | Hereditary retinal dystrophy | MGI |
| H35.50 | ICD10CM | Unspecified hereditary retinal dystrophy | MGI |
| H35.51 | ICD10CM | Vitreoretinal dystrophy | MGI |
| H35.52 | ICD10CM | Pigmentary retinal dystrophy | MGI |
| H35.53 | ICD10CM | Other dystrophies primarily involving the sensory retina | MGI |
| H35.54 | ICD10CM | Dystrophies primarily involving the retinal pigment epithelium | MGI |
| H36 | ICD10CM | Retinal disorders in diseases classified elsewhere | MGI |
| 362.70 | ICD9CM | Hereditary retinal dystrophy, unspecified | MGI |
| 362.71 | ICD9CM | Retinal dystrophy in systemic or cerebroretinal lipidoses | MGI |
| 362.72 | ICD9CM | Retinal dystrophy in other systemic disorders and syndromes | MGI |
| 362.73 | ICD9CM | Vitreoretinal dystrophies | MGI |
| 362.74 | ICD9CM | Pigmentary retinal dystrophy | MGI |
| 362.75 | ICD9CM | Other dystrophies primarily involving the sensory retina | MGI |
| 362.76 | ICD9CM | Dystrophies primarily involving the retinal pigment epithelium | MGI |
| 362.77 | ICD9CM | Dystrophies primarily involving Bruch's membrane | MGI |
| H35.5 | ICD10 | H35.5 Hereditary retinal dystrophy | UKB |
| 362.7 | ICD9 | 3627 Hereditary retinal dystrophies | UKB |
| 362.70 | ICD9 | 36270 Hereditary retinal dystrophies (retinitis pigmentosa) | UKB |
| 362.71 | ICD9 | 36271 Hereditary retinal dystrophies (batten's) | UKB |
| 362.72 | ICD9 | 36272 Hereditary retinal dystrophies (leber's) | UKB |
| 362.73 | ICD9 | 36273 Hereditary retinal dystrophies (lipofuscinosis, not otherwise specified) | UKB |
| 362.75 | ICD9 | 36275 Hereditary retinal dystrophies (tapetoretinal dystrophy) | 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.