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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
Athabaskan brainstem dysgenesis 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
Athabaskan brainstem dysgenesis syndrome
HOXA1



Fatal familial insomnia
Athabaskan brainstem dysgenesis syndrome

Synonym(s):
(no synonyms)

Synonym(s):
- ABSD
- Athabascan brainstem dysgenesis syndrome
- Navajo brainstem syndrome

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

Classification (ICD10):
- Certain infectious and parasitic diseases -
Classification (ICD10):
(no data available)

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 -
1 MeSH reference: C535397

No signs/symptoms info available.