Disease #00485 (OA1 (albinism, ocular, type I (OA-1,Nettleship-Falls type)), OMIM:300500)
| Official abbreviation |
OA1 |
| Name |
albinism, ocular, type I (OA-1,Nettleship-Falls type) |
| OMIM ID |
300500 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
X-linked |
| Individuals reported having this disease |
9 |
| Phenotype entries for this disease |
7 |
| Associated with 1 gene |
GPR143 |
| Associated tissues |
eyes |
| Disease features |
- |
| Remarks |
- |
| Date created |
2014-07-24 23:05:27 +02:00 (CEST) |
| Date last edited |
2021-12-10 21:51:32 +01:00 (CET) |
Individuals
|