Heinz body anemia
Information
- Disease name
- Heinz body anemia
- Disease ID
- DOID:0111363
- Description
- "A congenital nonspherocytic hemolytic anemia characterized by nonspherocytic hemolytic anemia of Dacie type I with Heinz bodies seen in erythrocytes after splenectomy that has_material_basis_in heterozygous mutation in the HBA1, HBA2 or HBB genes on chromosome 11p15.4, 16p13.3, and 16p13.3, respectively." [url:https\://www.ncbi.nlm.nih.gov/pubmed/14184033, url:https\://www.ncbi.nlm.nih.gov/pubmed/3997544, url:https\://www.ncbi.nlm.nih.gov/pubmed/8704193]
Disease area statistics
[No Data.]
Chromosome band
[No Data.]
Annotation
| Genes | Mutation | Description | Source | Links |
|---|
- Disase is a (Disease Ontology)
- DOID:2861
- Cross Reference ID (Disease Ontology)
- GARD:10718
- Cross Reference ID (Disease Ontology)
- MIM:140700
- HPO Human Phenotype ID (Human Phenotype Ontology)
- HP:0005511
- MedGen concept unique identifier (MedGen Concept name)
- C0700299
- MedGen unique identifier (MedGen Concept name)
- 148583