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Familial hemophagocytic lymphohistiocytosis
5 OMIM references -
4 associated genes
No signs/symptoms info
PROTEIN INTERACTIONS: 1
Hereditary cerebral hemorrhage with amyloidosis, Flemish type
1 OMIM reference -
1 associated gene
No signs/symptoms info
Familial hemophagocytic lymphohistiocytosis
Hereditary cerebral hemorrhage with amyloidosis, Flemish type

PRF1
(UniProt - OMIM)
 APP
(UniProt - OMIM)
STX11
(UniProt - OMIM)
STXBP2
(UniProt - OMIM)
UNC13D
(UniProt - OMIM)

INTERACTOME
ASSOCIATIONS
(click on a score value to see the evidence)
STX11
(0.56)
APP


Citations in the biomedical literature:


Familial hemophagocytic lymphohistiocytosis
PRF1 STX11 STXBP2 UNC13D
Hereditary cerebral hemorrhage with amyloidosis, Flemish type
APP



Familial hemophagocytic lymphohistiocytosis
Hereditary cerebral hemorrhage with amyloidosis, Flemish type

Synonym(s):
- Familial HLH
Synonym(s):
- HCHWA, Flemish type
Classification (Orphanet):
- Rare genetic disease
- Rare immune disease
- Rare neurologic disease
Classification (Orphanet):
- Rare genetic disease
- Rare neurologic disease
- Rare systemic or rheumatologic disease
Classification (ICD10):
- Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism -
Classification (ICD10):
(no data available)
Epidemiological data:
Class of prevalence: unknown
Average age onset: neonatal/infancy
Average age of death: -
Type of inheritance: autosomal recessive
Epidemiological data:
(no data available)
External references:
5 OMIM references -
No MeSH references
External references:
1 OMIM reference -
No MeSH references
No signs/symptoms info available.