Sialidosis Type 2
| Disease Aliases (21) | Cherry red spot--myoclonus syndrome Deficiency of neuraminidase Deficiency of sialidase Dysmorphic sialidosis Dysmorphic sialidosis with renal involvement Glycoprotein neuraminidase deficiency Infantile dysmorphic sialidosis Lipomucopolysaccharidosis Ml i Mucolipidosis type 1 Nephrosialidosis Neu 1 deficiency Neu deficiency Neu1 sialidosis Neug deficiency Neuraminidase 1 deficiency Neuraminidase deficiency Sialidase deficiency Sialidosis caused by mutation in neu1 Sialidosis type ii Sialidosis, type i |
Associated Genes (0) | |||||||
| Cross-references of Sialidosis type 2 | OMIM | GARD | Orphanet | NCBI-GTR | NCBI-MedGen | MalaCards | MeSH | Annotations | |