Disease #05364 (GPIBD15 (glycosylphosphatidylinositol biosynthesis defect, type 15 (GPIBD-15)), OMIM:617810)
| Official abbreviation |
GPIBD15 |
| Name |
glycosylphosphatidylinositol biosynthesis defect, type 15 (GPIBD-15) |
| OMIM ID |
617810 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
Autosomal recessive |
| Individuals reported having this disease |
- |
| Phenotype entries for this disease |
- |
| Associated with 1 gene |
GPAA1 |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2017-12-29 14:39:07 +01:00 (CET) |
| Date last edited |
2021-12-10 21:51:32 +01:00 (CET) |
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