Disease #00013 (Sialidosis (Neuraminidase Deficiency), OMIM:256550)
| Official abbreviation |
Sialidosis |
| Name |
Neuraminidase Deficiency |
| OMIM ID |
256550 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
Autosomal recessive |
| Individuals reported having this disease |
1 |
| Phenotype entries for this disease |
- |
| Associated with 1 gene |
NEU1 |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2020-12-21 00:34:06 +00:00 (UTC) |
| Date last edited |
N/A |
Individuals
|