Congenital Afibrinogenemia(Congenital fibrinogen deficiency) Explore Disorder's Alias
An Autosomal recessive mode(s) within the Blood disorders category
Candidate Gene Information
An Autosomal recessive mode(s) within the Blood disorders category
Reported Pathogenic variants
| S.No. | Name/GeneID | Description | Cytogentic Band | Gene Location on genomic DNA | Gene Length | Exons | Details | Gene Cross-References |
| 1 | FGG/2266 | fibrinogen gamma chain | 4q32.1 | Chr4, NC_000004.12 (154604136..154612656, complement) |
8521 nt | 10 | More... | OMIM gene gnomAD browser EnsEMBL GeneCards ClinGen gene |
| 2 | FGB/2244 | fibrinogen beta chain | 4q31.3 | Chr4, NC_000004.12 (154562980..154572807) |
9828 nt | 8 | More... | OMIM gene gnomAD browser EnsEMBL GeneCards ClinGen gene |
| 3 | FGA/2243 | fibrinogen alpha chain | 4q31.3 | Chr4, NC_000004.12 (154583126..154590742, complement) |
7617 nt | 6 | More... | OMIM gene gnomAD browser EnsEMBL GeneCards ClinGen gene |
| Variant Information | ||||||||
| Disorder Cross-References: Orphanet OMIM GARD GTR MedGen MalaCards EMBL-EBI OLS Monarch Initiative NORD | ||||||||
Patient care services
Clinical Symptoms & Disabilities
Prevalence
| Under development |