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Fatal post-viral neurodegenerative disorder
1 associated gene
4 connected diseases
No signs/symptoms info
Disease Type of connection
Familial hemophagocytic lymphohistiocytosis
Idiopathic aplastic anemia
Essential thrombocythemia
Myelofibrosis with myeloid metaplasia
Synonym(s):
(no synonyms)
Classification (Orphanet):
- Rare genetic disease
- Rare neurologic disease
Classification (ICD10):
(no data available)
Epidemiological data:
Class of prevalence: <1 / 1 000 000
Average age onset: childhood
Average age of death: child / adolescent
Type of inheritance: autosomal recessive
External references:
No OMIM references
No MeSH references
Gene symbol UniProt reference OMIM reference
PRF1 P14222170280
No signs/symptoms info available.