Hemoglobin H Disease
Disease ID: disease_node_17083
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| Dbxref | ICD10CM:D56.0, MIM:613978, ORDO:93616 |
|---|---|
| Subclassof | DOID_1099 |
| Data Source | DOID |
| Synonyms | HBH, alpha thalassemia, haemoglobin H type, alpha thalassemia, hemoglobin H type, alpha-thalassemia intermedia, haemoglobin H disease, haemoglobin H disease, deletional, hemoglobin H disease, deletional |
| Doid Label | hemoglobin H disease |
| Doid Description | An alpha thalassemia that has_material_basis_in contiguous gene deletion of the hemoglobin alpha-1 (HBA1) and alpha-2 (HBA2) genes on one chromosome 16, and a defect, deletional or nondeletional, in either HBA1 or HBA2 on the other. |
| Disease Node Id | disease_node_17083 |
| Doid Id | DOID_0110031 |
| Label | Hemoglobin H Disease |
- Outgoing r'ship
SUBCLASS_OFto/from Alpha-Thalassemia(ID:disease_node_9018) (Disease)