Disease #00492 (HPS9 (Hermansky-Pudlak syndrome, type 9 (HPS-9)), OMIM:614171)
| Official abbreviation |
HPS9 |
| Name |
Hermansky-Pudlak syndrome, type 9 (HPS-9) |
| OMIM ID |
614171 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
Autosomal recessive |
| Individuals reported having this disease |
- |
| Phenotype entries for this disease |
- |
| Associated with 1 gene |
BLOC1S6 |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2014-07-25 12:41:51 +02:00 (CEST) |
| Date last edited |
2021-12-10 21:51:32 +01:00 (CET) |
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