Disease #00479 (OCA3 (albinism, oculocutaneous, type III (OCA-3)), OMIM:203290)
| Official abbreviation |
OCA3 |
| Name |
albinism, oculocutaneous, type III (OCA-3) |
| OMIM ID |
203290 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
Autosomal recessive |
| Individuals reported having this disease |
9 |
| Phenotype entries for this disease |
7 |
| Associated with 1 gene |
TYRP1 |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2014-07-24 22:04:08 +02:00 (CEST) |
| Date last edited |
2021-12-10 21:51:32 +01:00 (CET) |
Individuals
|