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

ASPSCR1 APP
CLTC
NONO
PRCC
SFPQ
TFE3
TFEB


INTERACTOME
ASSOCIATIONS

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



Citations in the biomedical literature:


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



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

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

Synonym(s):
- HCHWA, Dutch type
- HCHWA-D

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

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

Epidemiological data:
(no data available)
Epidemiological data:
Class of prevalence: <1 / 1 000 000
Average age onset: adulthood
Average age of death: adult
Type of inheritance: autosomal dominant

External references:
1 OMIM reference -
No MeSH references
External references:
1 OMIM reference -
2 MeSH references: C537944 / D028243

Hereditary cerebral hemorrhage with amyloidosis, Dutch type

Very frequent
- Facial pain / cephalalgia / migraine
- Intracranial / cerebral / meningeal hemorrhage
- Psychic / behavioural troubles
- Psychic / psychomotor regression / dementia / intellectual decline

Frequent
- Intracranial / cerebral calcifications
- Seizures / epilepsy / absences / spasms / status epilepticus
- Transient cerebral ischemia / stroke

Occasional
- Early death / lethality


Translocation renal cell carcinoma

(no data available)