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1 OMIM reference -
1 associated gene
3 signs/symptoms
PROTEIN INTERACTIONS: 1
Hereditary cerebral hemorrhage with amyloidosis, Arctic type
Symptomatic form of muscular dystrophy of Duchenne and Becker in female carriers

APP DMD


INTERACTOME
ASSOCIATIONS

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



Citations in the biomedical literature:


Hereditary cerebral hemorrhage with amyloidosis, Arctic type
APP
Symptomatic form of muscular dystrophy of Duchenne and Becker in female carriers
DMD



Hereditary cerebral hemorrhage with amyloidosis, Arctic type
Symptomatic form of muscular dystrophy of Duchenne and Becker in female carriers

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 cardiac 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:
Class of prevalence: unknown
Average age onset: adulthood
Average age of death: -
Type of inheritance: x-linked dominant

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



Symptomatic form of muscular dystrophy of Duchenne and Becker in female carriers

(no data available)