Details
| Type | Protein Coding |
| Official Symbol | CFB |
| Official Name | complement factor B [Source:HGNC Symbol;Acc:HGNC:1037] |
| Ensembl ID | ENSG00000243649 |
| Bio databases IDs | |
| Aliases | complement factor B |
| Species | Human, Homo sapiens |
Top Findings
The most significant associations for this gene, including commonly observed domains, pathway involvement, and functional highlights based on current data.
phenotypes
- Atypical hemolytic uremic syndrome with complement gene abnormality
- NON RARE IN EUROPE: Age-related macular degeneration
- COMPLEMENT FACTOR B DEFICIENCY
- HEMOLYTIC UREMIC SYNDROME ATYPICAL SUSCEPTIBILITY TO 4
- MACULAR DEGENERATION AGE-RELATED 14