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1 OMIM reference -
1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 1
1 associated gene
No signs/symptoms info
Hereditary cerebral hemorrhage with amyloidosis, Flemish type
Mowat-Wilson syndrome due to a point mutation

APP ZEB2


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
APP
(0.56)
ZEB2



Citations in the biomedical literature:


Hereditary cerebral hemorrhage with amyloidosis, Flemish type
APP
Mowat-Wilson syndrome due to a point mutation
ZEB2



Hereditary cerebral hemorrhage with amyloidosis, Flemish type
Mowat-Wilson syndrome due to a point mutation

Synonym(s):
- HCHWA, Flemish type

Synonym(s):
- Hirschsprung disease and intellectual deficit due to a point mutation

Classification (Orphanet):
- Rare genetic disease
- Rare neurologic disease
- Rare systemic or rheumatologic disease
Classification (Orphanet):
- Rare abdominal surgical disease
- Rare developmental defect during embryogenesis
- Rare genetic disease
- Rare neurologic disease

Classification (ICD10):
(no data available)
Classification (ICD10):
- Congenital malformations, deformations and chromosomal abnormalities -

Epidemiological data:
(no data available)
Epidemiological data:
(no data available)

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

No signs/symptoms info available.