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Intermediate severe Salla disease
1 associated gene
No signs/symptoms info
COMMON GENES: 1
Free sialic acid storage disease, infantile form
1 OMIM reference -
1 associated gene
No signs/symptoms info
Intermediate severe Salla disease
Free sialic acid storage disease, infantile form

SLC17A5
(UniProt - OMIM)
 SLC17A5
(UniProt - OMIM)

COMMON
GENES 		SLC17A5


Citations in the biomedical literature:


Intermediate severe Salla disease
SLC17A5
Free sialic acid storage disease, infantile form



Intermediate severe Salla disease
Free sialic acid storage disease, infantile form

Synonym(s):
(no synonyms)

Synonym(s):
- ISSD
Classification (Orphanet):
- Inborn errors of metabolism
- Rare genetic 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.