Disease #00481 (OCA4 (albinism, oculocutaneous, type IV (OCA-4)), OMIM:606574)
| Official abbreviation |
OCA4 |
| Name |
albinism, oculocutaneous, type IV (OCA-4) |
| OMIM ID |
606574 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
Autosomal recessive |
| Individuals reported having this disease |
2 |
| Phenotype entries for this disease |
- |
| Associated with 1 gene |
SLC45A2 |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2014-07-24 22:24:28 +02:00 (CEST) |
| Date last edited |
2021-12-10 21:51:32 +01:00 (CET) |
Individuals
|