Disease #00490 (HPS5 (Hermansky-Pudlak syndrome, type 5 (HPS-5)), OMIM:614074)
| Official abbreviation |
HPS5 |
| Name |
Hermansky-Pudlak syndrome, type 5 (HPS-5) |
| OMIM ID |
614074 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
Autosomal recessive |
| Individuals reported having this disease |
1 |
| Phenotype entries for this disease |
1 |
| Associated with 1 gene |
HPS5 |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2014-07-25 12:30:29 +02:00 (CEST) |
| Date last edited |
2021-12-10 21:51:32 +01:00 (CET) |
Individuals
|