inherited hemoglobinopathy
MONDO:0019050Mondo
Findings
No curated finding names inherited hemoglobinopathy yet. Everything below is reference data from Mondo, HPO and GenCC, not evidence about what affects it.
Definition
An inherited disorder characterized by structural alterations of a globin chain within the hemoglobin molecule.
Definition from the Mondo Disease Ontology (MONDO:0019050), read 2026-09-29. CC BY 4.0.
Where it sits
- A kind of
- Narrower terms (17)
- beta-thalassemia and related diseases
- congenital nonspherocytic hemolytic anemia
- hemoglobin C disease
- hemoglobin D disease
- hemoglobin E disease
- hemoglobinopathy Toms River
- hereditary methemoglobinemia
- hereditary persistence of fetal hemoglobin
- hereditary persistence of fetal hemoglobin-sickle cell disease syndrome
- homozygous hemoglobin O Arab disease
- sickle cell disease
- sickle cell-beta-thalassemia disease syndrome
- sickle cell-hemoglobin d disease syndrome
- sickle cell-hemoglobin E disease syndrome
- sulfhemoglobinemia, congenital
- thalassemia
- unstable hemoglobin disease
Other names
2 names
Resolves to: inherited hemoglobinopathy
- Also called
- Hemoglobinopathies / iron metabolismhereditary hemoglobinopathy