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1 OMIM reference -
1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 1
1 OMIM reference -
1 associated gene
No signs/symptoms info
Fatal familial insomnia
Bosley-Salih-Alorainy syndrome

PRNP HOXA1


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
PRNP
(0.78)
HOXA1



Citations in the biomedical literature:


Fatal familial insomnia
PRNP
Bosley-Salih-Alorainy syndrome
HOXA1



Fatal familial insomnia
Bosley-Salih-Alorainy syndrome

Classification (Orphanet):
- Rare genetic disease
- Rare neurologic disease
Classification (Orphanet):
- Rare developmental defect during embryogenesis
- Rare genetic disease
- Rare otorhinolaryngologic disease
- Rare surgical cardiac disease

Classification (ICD10):
- Certain infectious and parasitic diseases -
Classification (ICD10):
- Congenital malformations, deformations and chromosomal abnormalities -

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: <1 / 1 000 000
Average age onset: neonatal/infancy
Average age of death: no data available
Type of inheritance: autosomal recessive

External references:
1 OMIM reference -
1 MeSH reference: D034062
External references:
1 OMIM reference -
No MeSH references

No signs/symptoms info available.