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1 OMIM reference -
2 associated genes
No signs/symptoms info
PROTEIN INTERACTIONS: 1
1 OMIM reference -
1 associated gene
No signs/symptoms info
Alveolar soft-part sarcoma
Hereditary cerebral hemorrhage with amyloidosis, Flemish type

ASPSCR1 APP
TFE3


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
ASPSCR1
(0.56)
APP



Citations in the biomedical literature:


Alveolar soft-part sarcoma
ASPSCR1 TFE3
Hereditary cerebral hemorrhage with amyloidosis, Flemish type
APP



Alveolar soft-part sarcoma
Hereditary cerebral hemorrhage with amyloidosis, Flemish type

Synonym(s):
(no synonyms)

Synonym(s):
- HCHWA, Flemish type

Classification (Orphanet):
- Rare oncologic disease
Classification (Orphanet):
- Rare genetic disease
- Rare neurologic disease
- Rare systemic or rheumatologic disease

Classification (ICD10):
(no data available)
Classification (ICD10):
(no data available)

Epidemiological data:
(no data available)
Epidemiological data:
(no data available)

External references:
1 OMIM reference -
1 MeSH reference: D018234
External references:
1 OMIM reference -
No MeSH references

No signs/symptoms info available.