HAMP
HGNC:15598 · SaudiVarKB evidence summary derived from retained literature mentions.
3Gene mentions
3Publications
1Linked variants
2Associated phenotypes
Associated phenotypes
Co-mentioned in HAMP publications| Phenotype | Identifier | Articles | Mentions |
|---|---|---|---|
| cardiomyopathy | HP:0001638 | 1 | 1 |
| hepatocellular carcinoma | — | 1 | 1 |
Linked variants
Variants normalized to HAMP| Variant | HGVS / rsID | Articles | Mentions |
|---|---|---|---|
| rs10421768 | rs10421768 | 1 | 1 |
Population context
Reported in the same publications| Country / region | Group | Cohort | Articles |
|---|---|---|---|
| Asir | — | — | 1 |
| Saudi Arabia · Tabuk | — | 108 | 1 |
Supporting publications
3 records- 2021Juvenile Hemochromatosis: Rheumatic Manifestations of 2 Sisters Responding to Deferasirox Treatment. A Case Series and Literature Review.Open access rheumatology : research and reviewsPubMed ↗
- 2021Frequency of the HAMP (c.-582 A>G) Polymorphism in Iron Deficiency in Saudi Arabia.Pakistan journal of biological sciences : PJBSPubMed ↗
- 2017Juvenile hemochromatosis and hepatocellular carcinoma in a patient with a novel mutation in the HJV gene.European journal of medical geneticsPubMed ↗