Disease #00165 (SCD (Sickle Cell Anemia), OMIM:603903)
| Official abbreviation |
SCD |
| Name |
Sickle Cell Anemia |
| OMIM ID |
603903 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
Autosomal recessive |
| Individuals reported having this disease |
1 |
| Phenotype entries for this disease |
1 |
| Associated with 1 gene |
HBB |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2022-04-11 12:29:15 +00:00 (UTC) |
| Date last edited |
N/A |
Individuals
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