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 |
- |
Individuals
|
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