hemochromatosis type 2B
Information
- Disease name
- hemochromatosis type 2B
- Disease ID
- DOID:0111032
- Description
- "A hemochromatosis type 2 that has_material_basis_in homozygous mutation in the HAMP gene on chromosome 19q13." [url:https\://www.ncbi.nlm.nih.gov/pubmed/12469120]
Disease area statistics
[No Data.]
Chromosome band
[No Data.]
Annotation
| Genes | Mutation | Description | Source | Links |
|---|
- Disase is a (Disease Ontology)
- DOID:0111034
- Cross Reference ID (Disease Ontology)
- MIM:613313
- Exact Synonym (Disease Ontology)
- HFE2B
- MedGen concept unique identifier (MedGen Concept name)
- C1865616
- MedGen unique identifier (MedGen Concept name)
- 356040