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- NCIT_C178648 IAO_0000115 "Human CFB wild-type allele is located in the vicinity of 6p21.33 and is approximately 6 kb in length. This allele, which encodes complement factor B protein, is involved in convertase activity associated with complement activation. Mutation of the gene is associated with complement deficiency, decreased risk for age-related macular degeneration and increased susceptibility to atypical hemolytic uremic syndrome." @default.
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- NCIT_C178648 NCIT_P106 "Gene or Genome" @default.
- NCIT_C178648 NCIT_P108 "CFB wt Allele" @default.
- NCIT_C178648 NCIT_P208 "CL1648288" @default.
- NCIT_C178648 NCIT_P321 "629" @default.
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- NCIT_C178648 hasExactSynonym "AHUS4" @default.
- NCIT_C178648 hasExactSynonym "ARMD14" @default.
- NCIT_C178648 hasExactSynonym "B-Factor, Properdin Gene" @default.
- NCIT_C178648 hasExactSynonym "BF" @default.
- NCIT_C178648 hasExactSynonym "BFD" @default.
- NCIT_C178648 hasExactSynonym "CFAB" @default.
- NCIT_C178648 hasExactSynonym "CFB wt Allele" @default.
- NCIT_C178648 hasExactSynonym "CFBD" @default.
- NCIT_C178648 hasExactSynonym "Complement Factor B wt Allele" @default.
- NCIT_C178648 hasExactSynonym "FB" @default.
- NCIT_C178648 hasExactSynonym "FBI12" @default.
- NCIT_C178648 hasExactSynonym "GBG" @default.
- NCIT_C178648 hasExactSynonym "H2-Bf" @default.
- NCIT_C178648 hasExactSynonym "PBF2" @default.
- NCIT_C178648 type Class @default.
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- NCIT_C178648 label "CFB wt Allele" @default.
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