Autoimmune Hemolytic Anemia(AHA)
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 | SOCS1/8651 | suppressor of cytokine signaling 1 | 16p13.13 | Chr16, NC_000016.10 (11254417..11256204, complement) |
1788 nt | 2 | More... | OMIM gene gnomAD browser EnsEMBL GeneCards ClinGen gene |
| 2 | TLR8/51311 | toll like receptor 8 | Xp22.2 | ChrX, NC_000023.11 (12906620..12923169) |
16550 nt | 3 | More... | OMIM gene gnomAD browser EnsEMBL GeneCards ClinGen gene |
| Variant Information | ||||||||
| Disorder Cross-References: GTR MalaCards NORD | ||||||||
Patient care services
Clinical Symptoms & Disabilities
Prevalence
| Under development |