Disease #00245 (Ii (blood group antigen i (BG-i)), OMIM:110800)
| Official abbreviation |
Ii |
| Name |
blood group antigen i (BG-i) |
| OMIM ID |
110800 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
Autosomal dominant |
| Individuals reported having this disease |
17 |
| Phenotype entries for this disease |
13 |
| Associated with 1 gene |
GCNT2 |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2013-10-13 16:10:24 +02:00 (CEST) |
| Date last edited |
2021-12-10 21:51:32 +01:00 (CET) |
Individuals
|