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Familial encephalopathy with neuroserpin inclusion bodies
1 OMIM reference -
1 associated gene
2 connected diseases
No signs/symptoms info
Disease Type of connection
Hypoplasminogenemia
Ligneous conjunctivitis
Synonym(s):
- FENIB
Classification (Orphanet):
- Rare genetic disease
- Rare neurologic disease
Classification (ICD10):
- Diseases of the nervous system -
Epidemiological data:
Class of prevalence: <1 / 1 000 000
Average age onset: adulthood
Average age of death: -
Type of inheritance: autosomal dominant
External references:
1 OMIM reference -
1 MeSH reference: C536841
Gene symbol UniProt reference OMIM reference
SERPINI1 Q99574602445
No signs/symptoms info available.