Cytoscape Web
Click node...


1 OMIM reference -
1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 1
1 OMIM reference -
2 associated genes
No signs/symptoms info
Hereditary cerebral hemorrhage with amyloidosis, Flemish type
Mitochondrial trifunctional protein deficiency

APP HADHA
HADHB


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
APP
(0.62)
HADHB



Citations in the biomedical literature:


Hereditary cerebral hemorrhage with amyloidosis, Flemish type
APP
Mitochondrial trifunctional protein deficiency
HADHA HADHB



Hereditary cerebral hemorrhage with amyloidosis, Flemish type
Mitochondrial trifunctional protein deficiency

Synonym(s):
- HCHWA, Flemish type

Synonym(s):
- TFP deficiency
- TFPD

Classification (Orphanet):
- Rare genetic disease
- Rare neurologic disease
- Rare systemic or rheumatologic disease
Classification (Orphanet):
- Inborn errors of metabolism
- Rare cardiac disease
- Rare genetic disease
- Rare neurologic disease

Classification (ICD10):
(no data available)
Classification (ICD10):
- Diseases of the nervous system -

Epidemiological data:
(no data available)
Epidemiological data:
Class of prevalence: <1 / 1 000 000
Average age onset: neonatal/infancy
Average age of death: before age 5
Type of inheritance: autosomal recessive

External references:
1 OMIM reference -
No MeSH references
External references:
1 OMIM reference -
1 MeSH reference: D024741

No signs/symptoms info available.