Cytoscape Web
Click node...

Autosomal recessive spastic paraplegia type 54
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
Autosomal recessive spastic paraplegia type 54
Hereditary cerebral hemorrhage with amyloidosis, Flemish type

DDHD2
(UniProt - OMIM)
 APP
(UniProt - OMIM)

INTERACTOME
ASSOCIATIONS
(click on a score value to see the evidence)
DDHD2
(0.56)
APP


Citations in the biomedical literature:


Autosomal recessive spastic paraplegia type 54
DDHD2
Hereditary cerebral hemorrhage with amyloidosis, Flemish type
APP



Autosomal recessive spastic paraplegia type 54
Hereditary cerebral hemorrhage with amyloidosis, Flemish type

Synonym(s):
- SPG54
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.