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13 OMIM references -
14 associated genes
No signs/symptoms info
PROTEIN INTERACTIONS: 4
1 OMIM reference -
1 associated gene
3 signs/symptoms
Autosomal dominant nonsyndromic intellectual deficit
Hereditary cerebral hemorrhage with amyloidosis, Arctic type

CACNG2 APP
CDH15
CTNNB1
DOCK8
DYNC1H1
DYRK1A
EPB41L1
GRIN1
GRIN2B
KIF1A
KIRREL3
MBD5
SYNGAP1
TCF4


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
CACNG2
CTNNB1
DYRK1A
EPB41L1
(0.56)
(0.56)
(0.56)
(0.56)
APP
APP
APP
APP



Citations in the biomedical literature:


Autosomal dominant nonsyndromic intellectual deficit
CACNG2 CDH15 CTNNB1 DOCK8 DYNC1H1 DYRK1A
EPB41L1 GRIN1 GRIN2B KIF1A KIRREL3 MBD5
SYNGAP1 TCF4
Hereditary cerebral hemorrhage with amyloidosis, Arctic type
APP



Autosomal dominant nonsyndromic intellectual deficit
Hereditary cerebral hemorrhage with amyloidosis, Arctic type

Synonym(s):
(no synonyms)

Synonym(s):
- HCHWA, Arctic type

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

Classification (ICD10):
(no data available)
Classification (ICD10):
(no data available)

Epidemiological data:
Class of prevalence: -
Average age onset: -
Average age of death: -
Type of inheritance: autosomal dominant
Epidemiological data:
(no data available)

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

Hereditary cerebral hemorrhage with amyloidosis, Arctic type

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



Autosomal dominant nonsyndromic intellectual deficit

(no data available)