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

APP ANKS6
GLIS2
NPHP1
NPHP4
WDR19


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, Arctic type
APP
Juvenile autosomal recessive medullary cystic kidney disease
ANKS6 GLIS2 NPHP1 NPHP4 WDR19



Hereditary cerebral hemorrhage with amyloidosis, Arctic type
Juvenile autosomal recessive medullary cystic kidney disease

Synonym(s):
- HCHWA, Arctic 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:
Class of prevalence: -
Average age onset: -
Average age of death: -
Type of inheritance: autosomal recessive

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

Hereditary cerebral hemorrhage with amyloidosis, Arctic type

Very frequent
- Autosomal dominant inheritance
- Psychic / behavioural troubles
- Psychic / psychomotor regression / dementia / intellectual decline



Juvenile autosomal recessive medullary cystic kidney disease

(no data available)