H63D
H63D · SaudiVarKB evidence summary derived from retained literature mentions.
6Variant mentions
6Publications
9Associated gene records
4Associated phenotype records
Associated gene records
Co-mentioned in the same publicationsAssociated phenotype records
Co-mentioned in the same publications| Phenotype | Identifier / context | Articles | Mentions |
|---|---|---|---|
| diabetes mellitus | — | 2 | 2 |
| thalassemia | HP:0001878 | 2 | 2 |
| COVID-19 | — | 1 | 1 |
| SARS | — | 1 | 1 |
Associated population records
Co-mentioned in the same publications| Population | Identifier / context | Articles | Mentions |
|---|---|---|---|
| Population record | Cohort 2 | 1 | 1 |
| Population record | Cohort 204 | 1 | 1 |
| Saudi Arabia · Tabuk | Cohort 19 | 1 | 1 |
| Population record | Cohort 560 | 1 | 1 |
Supporting publications
6 records- 2024Whole-Exome Sequencing Detecting a Recurrent Pathogenic Mutation, HFE p.His63Asp (H63D) in COVID-19 Patients and Its Effect on Mortality.Discovery medicine1 mentions
- 2019Association of frequency of hereditary hemochromatosis (HFE) gene mutations (H63D and C282Y) with iron overload in beta-thalassemia major patients in Pakistan.Saudi medical journal1 mentions
- 2019Comment on: Hemochromatosis (HFE) gene mutations (H63D and C282Y) and iron overload in beta-thalassemia major.Saudi medical journal1 mentions
- 2013Correlation of hemochromatosis gene mutations and cardiovascular disease in hemodialysis patients.Annals of Saudi medicine1 mentions
- 2011Hereditary hemochromatosis of tongue.Oral surgery, oral medicine, oral pathology, oral radiology, and endodontics1 mentions
- 2008Hemochromatosis gene (HFE) mutations in patients with type 2 diabetes and their control group in an Iranian population.Saudi medical journal1 mentions