Disease #00153 (HH (Hereditary Hemochromatosis), OMIM:235200)
Official abbreviation |
HH |
Name |
Hereditary Hemochromatosis |
OMIM ID |
235200 |
Human Phenotype Ontology Project (HPO) |
HPO |
Inheritance |
Autosomal recessive |
Individuals reported having this disease |
3 |
Phenotype entries for this disease |
- |
Associated with 1 gene |
HFE |
Associated tissues |
- |
Disease features |
- |
Remarks |
- |
Individuals
|
|