Disease #00349 (CFID (deficiency, complement factor I), OMIM:610984)
| Official abbreviation |
CFID |
| Name |
deficiency, complement factor I |
| OMIM ID |
610984 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
Autosomal recessive |
| Individuals reported having this disease |
2 |
| Phenotype entries for this disease |
2 |
| Associated with 1 gene |
CFI |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2014-03-13 09:55:00 +01:00 (CET) |
| Date last edited |
2025-03-26 19:40:48 +01:00 (CET) |
Individuals
|