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
|