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Congenital sialidosis type 2
1 associated gene
No signs/symptoms info
COMMON GENES: 1
Juvenile sialidosis type 2
1 associated gene
No signs/symptoms info
Congenital sialidosis type 2
Juvenile sialidosis type 2

NEU1
(UniProt - OMIM)
 NEU1
(UniProt - OMIM)

COMMON
GENES 		NEU1


Citations in the biomedical literature:


Congenital sialidosis type 2
NEU1
Juvenile sialidosis type 2



Congenital sialidosis type 2
Juvenile sialidosis type 2

Classification (Orphanet):
- Inborn errors of metabolism
- Rare bone disease
- Rare developmental defect during embryogenesis
- Rare eye disease
- Rare genetic disease
- Rare neurologic disease
- Rare renal disease
Classification (Orphanet):
- Inborn errors of metabolism
- Rare bone disease
- Rare developmental defect during embryogenesis
- Rare eye disease
- Rare genetic disease
- Rare neurologic disease
- Rare renal disease
Classification (ICD10):
- Endocrine, nutritional and metabolic diseases -
Classification (ICD10):
- Endocrine, nutritional and metabolic diseases -
Epidemiological data:
(no data available)
Epidemiological data:
(no data available)
External references:
No OMIM references
No MeSH references
External references:
No OMIM references
No MeSH references
No signs/symptoms info available.