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Free sialic acid storage disease, infantile form
1 OMIM reference -
1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 1
Hereditary cerebral hemorrhage with amyloidosis, Flemish type
1 OMIM reference -
1 associated gene
No signs/symptoms info
Free sialic acid storage disease, infantile form
Hereditary cerebral hemorrhage with amyloidosis, Flemish type

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

INTERACTOME
ASSOCIATIONS
(click on a score value to see the evidence)
SLC17A5
(0.56)
APP


Citations in the biomedical literature:


Free sialic acid storage disease, infantile form
SLC17A5
Hereditary cerebral hemorrhage with amyloidosis, Flemish type
APP



Free sialic acid storage disease, infantile form
Hereditary cerebral hemorrhage with amyloidosis, Flemish type

Synonym(s):
- ISSD
Synonym(s):
- HCHWA, Flemish type
Classification (Orphanet):
- Inborn errors of metabolism
- Rare genetic disease
Classification (Orphanet):
- Rare genetic disease
- Rare neurologic disease
- Rare systemic or rheumatologic disease
Classification (ICD10):
- Endocrine, nutritional and metabolic diseases -
Classification (ICD10):
(no data available)
Epidemiological data:
(no data available)
Epidemiological data:
(no data available)
External references:
1 OMIM reference -
No MeSH references
External references:
1 OMIM reference -
No MeSH references
No signs/symptoms info available.