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Congenital sialidosis type 2
1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 1
Mucopolysaccharidosis type 4A
1 OMIM reference -
1 associated gene
No signs/symptoms info
Congenital sialidosis type 2
Mucopolysaccharidosis type 4A

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

INTERACTOME
ASSOCIATIONS
(click on a score value to see the evidence)
NEU1
(0.55)
GALNS


Citations in the biomedical literature:


Congenital sialidosis type 2
NEU1
Mucopolysaccharidosis type 4A
GALNS



Congenital sialidosis type 2
Mucopolysaccharidosis type 4A

Synonym(s):
(no synonyms)

Synonym(s):
- GALNS deficiency
- Galactosamine-6-sulfatase deficiency
- MPSIVA
- Morquio disease type A
- N-acetylgalactosamine-6-sulfate sulfatase deficiency
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 genetic 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:
1 OMIM reference -
No MeSH references
No signs/symptoms info available.