Disease #01561 (SPH1 (spherocytosis, type 1 (SPH1)), OMIM:182900)
| Official abbreviation |
SPH1 |
| Name |
spherocytosis, type 1 (SPH1) |
| OMIM ID |
182900 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
Autosomal dominant, Autosomal recessive |
| Individuals reported having this disease |
2 |
| Phenotype entries for this disease |
- |
| Associated with 2 genes |
ANK1, SPTA1 |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2014-09-25 23:29:40 +02:00 (CEST) |
| Date last edited |
2020-09-15 10:12:59 +02:00 (CEST) |
Individuals
|