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1 OMIM reference -
1 associated gene
3 signs/symptoms
PROTEIN INTERACTIONS: 1
5 OMIM references -
10 associated genes
No signs/symptoms info
Hereditary cerebral hemorrhage with amyloidosis, Arctic type
Postsynaptic congenital myasthenic syndromes

APP AGRN
CHRNA1
CHRNB1
CHRND
CHRNE
DOK7
LRP4
MUSK
RAPSN
SCN4A


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
APP
(0.52)
AGRN



Citations in the biomedical literature:


Hereditary cerebral hemorrhage with amyloidosis, Arctic type
APP
Postsynaptic congenital myasthenic syndromes
AGRN CHRNA1 CHRNB1 CHRND CHRNE DOK7
LRP4 MUSK RAPSN SCN4A



Hereditary cerebral hemorrhage with amyloidosis, Arctic type
Postsynaptic congenital myasthenic syndromes

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 eye 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:
(no data available)

External references:
1 OMIM reference -
No MeSH references
External references:
5 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



Postsynaptic congenital myasthenic syndromes

(no data available)