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1 OMIM reference -
1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 1
5 OMIM references -
5 associated genes
No signs/symptoms info
Fatal familial insomnia
Familial exudative vitreoretinopathy

PRNP FZD4
LRP5
NDP
TSPAN12
ZNF408


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
PRNP
(0.68)
ZNF408



Citations in the biomedical literature:


Fatal familial insomnia
PRNP
Familial exudative vitreoretinopathy
FZD4 LRP5 NDP TSPAN12 ZNF408



Fatal familial insomnia
Familial exudative vitreoretinopathy

Synonym(s):
(no synonyms)

Synonym(s):
- Criswick-Schepens syndrome
- FEVR

Classification (Orphanet):
- Rare genetic disease
- Rare neurologic disease
Classification (Orphanet):
- Rare eye disease
- Rare genetic disease
- Rare neurologic disease

Classification (ICD10):
- Certain infectious and parasitic diseases -
Classification (ICD10):
- Diseases of the eye and adnexa -

Epidemiological data:
Class of prevalence: <1 / 1 000 000
Average age onset: adulthood
Average age of death: -
Type of inheritance: autosomal dominant
Epidemiological data:
Class of prevalence: unknown
Average age onset: neonatal/infancy
Average age of death: any age
Type of inheritance: autosomal dominant

External references:
1 OMIM reference -
1 MeSH reference: D034062
External references:
5 OMIM references -
1 MeSH reference: C536382

No signs/symptoms info available.