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 -

  Powered by LOVD v.3.0 Build 28d
LOVD software ©2004-2023 Leiden University Medical Center 		There are currently no updates.