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1 OMIM reference -
1 associated gene
3 signs/symptoms
PROTEIN INTERACTIONS: 1
1 OMIM reference -
7 associated genes
No signs/symptoms info
Hereditary cerebral hemorrhage with amyloidosis, Arctic type
Translocation renal cell carcinoma

APP ASPSCR1
CLTC
NONO
PRCC
SFPQ
TFE3
TFEB


INTERACTOME
ASSOCIATIONS

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



Citations in the biomedical literature:


Hereditary cerebral hemorrhage with amyloidosis, Arctic type
APP
Translocation renal cell carcinoma
ASPSCR1 CLTC NONO PRCC SFPQ TFE3
TFEB



Hereditary cerebral hemorrhage with amyloidosis, Arctic type
Translocation renal cell carcinoma

Synonym(s):
- HCHWA, Arctic type

Synonym(s):
- Carcinoma associated with MITF/TFE translocation
- Translocation carcinoma

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

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

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

Hereditary cerebral hemorrhage with amyloidosis, Arctic type

Very frequent
- Autosomal dominant inheritance
- Psychic / behavioural troubles
- Psychic / psychomotor regression / dementia / intellectual decline



Translocation renal cell carcinoma

(no data available)