| Dataset | OMIM Gene-Disease Associations |
| Category | disease or phenotype associations |
| Type | phenotype |
| Description | Anemia characterized by abnormal intracellular inclusions, composed of denatured hemoglobin, found on the membrane of red blood cells. (Human Phenotype Ontology, HP_0005511) |
| External Link | http://www.omim.org/entry/140700 |
| Similar Terms | |
| Downloads & Tools |
1 genes associated with the heinz body anemia phenotype from the curated OMIM Gene-Disease Associations dataset.
| Symbol | Name |
|---|---|
| HBA2 | hemoglobin, alpha 2 |
