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1 OMIM reference -
1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 1
4 associated genes
No signs/symptoms info
Hereditary cerebral hemorrhage with amyloidosis, Flemish type
Infantile autosomal recessive medullary cystic kidney disease

APP ANKS6
INVS
NEK8
TTC21B


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
APP
(0.56)
ANKS6



Citations in the biomedical literature:


Hereditary cerebral hemorrhage with amyloidosis, Flemish type
APP
Infantile autosomal recessive medullary cystic kidney disease
ANKS6 INVS NEK8 TTC21B



Hereditary cerebral hemorrhage with amyloidosis, Flemish type
Infantile autosomal recessive medullary cystic kidney disease

Synonym(s):
- HCHWA, Flemish type

Synonym(s):
(no synonyms)

Classification (Orphanet):
- Rare genetic disease
- Rare neurologic disease
- Rare systemic or rheumatologic disease
Classification (Orphanet):
- Rare genetic disease
- Rare renal 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.