Disease #02373 (SW (blood group system, Swann system (SW)), OMIM:601550)
| Official abbreviation |
SW |
| Name |
blood group system, Swann system (SW) |
| OMIM ID |
601550 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
- |
| Individuals reported having this disease |
- |
| Phenotype entries for this disease |
- |
| Associated with 1 gene |
SLC4A1 |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2014-09-25 23:29:40 +02:00 (CEST) |
| Date last edited |
2016-03-20 12:15:43 +01:00 (CET) |
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