Cytoscape Web
Click node...

Neurodegeneration with brain iron accumulation due to C19orf12 mutation
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
Neurodegeneration with brain iron accumulation due to C19orf12 mutation
Hereditary cerebral hemorrhage with amyloidosis, Flemish type

C19ORF12
(UniProt - OMIM)
 APP
(UniProt - OMIM)

INTERACTOME
ASSOCIATIONS
(click on a score value to see the evidence)
C19ORF12
(0.56)
APP


Citations in the biomedical literature:


Neurodegeneration with brain iron accumulation due to C19orf12 mutation
C19ORF12
Hereditary cerebral hemorrhage with amyloidosis, Flemish type
APP



Neurodegeneration with brain iron accumulation due to C19orf12 mutation
Hereditary cerebral hemorrhage with amyloidosis, Flemish type

Synonym(s):
- MPAN
- Mitochondrial membrane protein associated neurodegeneration
- NBIA due to C19orf12 mutation
- NBIA5
- Neurodegeneration with brain iron accumulation type 5
Synonym(s):
- HCHWA, Flemish type
Classification (Orphanet):
- Rare eye disease
- 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:
Class of prevalence: unknown
Average age onset: childhood
Average age of death: -
Type of inheritance: autosomal recessive
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.