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 |
0 |
Associated with 1 gene |
NEU1 |
Associated tissues |
- |
Disease features |
- |
Remarks |
- |
Individuals
|
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