Congenital pigmentary anomalies of skin
691.3
Dermatologic
Both
690-697.99
ICD mappings
| ICD code | Type | Description | Phenome |
|---|---|---|---|
| Q82.1 | ICD10CM | Xeroderma pigmentosum | MGI |
| Q82.2 | ICD10CM | Congenital cutaneous mastocytosis | MGI |
| Q82.3 | ICD10CM | Incontinentia pigmenti | MGI |
| 757.33 | ICD9CM | Congenital pigmentary anomalies of skin | MGI |
| Q82.1 | ICD10 | Q82.1 Xeroderma pigmentosum | UKB |
| Q82.2 | ICD10 | Q82.2 Mastocytosis | UKB |
| 757.33 | ICD9 | 75733 Other specified anomalies of skin (epidermolysis bullosa) | 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.