Disease #01203 (blood group P (blood group system, P1PK), OMIM:111400)
| Official abbreviation |
blood group P |
| Name |
blood group system, P1PK |
| OMIM ID |
111400 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
- |
| Individuals reported having this disease |
- |
| Phenotype entries for this disease |
- |
| Associated with 2 genes |
A4GALT, B3GALNT1 |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2014-09-25 23:29:40 +02:00 (CEST) |
| Date last edited |
2015-12-08 23:50:05 +01:00 (CET) |
|
Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.
|