Cytoscape Web
Click node...

Beta-propeller protein-associated neurodegeneration
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
Beta-propeller protein-associated neurodegeneration
Hereditary cerebral hemorrhage with amyloidosis, Flemish type

WDR45
(UniProt - OMIM)
 APP
(UniProt - OMIM)

INTERACTOME
ASSOCIATIONS
(click on a score value to see the evidence)
WDR45
(0.56)
APP


Citations in the biomedical literature:


Beta-propeller protein-associated neurodegeneration
WDR45
Hereditary cerebral hemorrhage with amyloidosis, Flemish type
APP



Beta-propeller protein-associated neurodegeneration
Hereditary cerebral hemorrhage with amyloidosis, Flemish type

Synonym(s):
- BPAN
- NBIA4
- Neurodegeneration with brain iron accumulation type 4
- SENDA
- Static encephalopathy of childhood with neurdegeneration in adulthood
Synonym(s):
- HCHWA, Flemish type
Classification (Orphanet):
- Rare genetic disease
- Rare neurologic disease
Classification (Orphanet):
- Rare genetic disease
- Rare neurologic disease
- Rare systemic or rheumatologic disease
Classification (ICD10):
- Diseases of the nervous system -
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.