Disease #02879 (ECYT3 (erythrocytosis, familial, type 3 (ECYT-3)), OMIM:609820)
Official abbreviation |
ECYT3 |
Name |
erythrocytosis, familial, type 3 (ECYT-3) |
OMIM ID |
609820 |
Human Phenotype Ontology Project (HPO) |
HPO |
Inheritance |
Autosomal dominant |
Individuals reported having this disease |
- |
Phenotype entries for this disease |
- |
Associated with 1 gene |
EGLN1 |
Associated tissues |
- |
Disease features |
- |
Remarks |
- |
|
|