Disease #03207 (AHUS5 (hemolyticuremic syndrome, atypical, susceptibility type 5 (AHUS5)), OMIM:612925)
| Official abbreviation |
AHUS5 |
| Name |
hemolyticuremic syndrome, atypical, susceptibility type 5 (AHUS5) |
| OMIM ID |
612925 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
Autosomal dominant |
| Individuals reported having this disease |
- |
| Phenotype entries for this disease |
- |
| Associated with 1 gene |
C3 |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2014-09-25 23:29:40 +02:00 (CEST) |
| Date last edited |
2022-01-07 11:58:28 +01:00 (CET) |
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