Cytoscape Web
Click node...

Persistent hyperplastic primary vitreous
2 OMIM references -
3 associated genes
No signs/symptoms info
PROTEIN INTERACTIONS: 1
Hereditary cerebral hemorrhage with amyloidosis, Flemish type
1 OMIM reference -
1 associated gene
No signs/symptoms info
Persistent hyperplastic primary vitreous
Hereditary cerebral hemorrhage with amyloidosis, Flemish type

ATOH7
(UniProt - OMIM)
 APP
(UniProt - OMIM)
FZD4
(UniProt - OMIM)
NDP
(UniProt - OMIM)

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


Citations in the biomedical literature:


Persistent hyperplastic primary vitreous
ATOH7 FZD4 NDP
Hereditary cerebral hemorrhage with amyloidosis, Flemish type
APP



Persistent hyperplastic primary vitreous
Hereditary cerebral hemorrhage with amyloidosis, Flemish type

Synonym(s):
- PFVS
- PHPV
- Persistent fetal vasculature syndrome
Synonym(s):
- HCHWA, Flemish type
Classification (Orphanet):
- Rare eye disease
- Rare genetic disease
Classification (Orphanet):
- Rare genetic disease
- Rare neurologic disease
- Rare systemic or rheumatologic disease
Classification (ICD10):
- Congenital malformations, deformations and chromosomal abnormalities -
Classification (ICD10):
(no data available)
Epidemiological data:
Class of prevalence: unknown
Average age onset: neonatal/infancy
Average age of death: -
Type of inheritance: autosomal dominant
Epidemiological data:
(no data available)
External references:
2 OMIM references -
1 MeSH reference: D054514
External references:
1 OMIM reference -
No MeSH references
No signs/symptoms info available.