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

APP SLC17A5


INTERACTOME
ASSOCIATIONS

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



Citations in the biomedical literature:


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



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

Synonym(s):
- HCHWA, Flemish type

Synonym(s):
- ISSD

Classification (Orphanet):
- Rare genetic disease
- Rare neurologic disease
- Rare systemic or rheumatologic disease
Classification (Orphanet):
- Inborn errors of metabolism
- Rare genetic disease

Classification (ICD10):
(no data available)
Classification (ICD10):
- Endocrine, nutritional and metabolic diseases -

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.