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1 OMIM reference -
1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 1
1 OMIM reference -
1 associated gene
3 signs/symptoms
Autosomal dominant spastic paraplegia type 13
Hereditary cerebral hemorrhage with amyloidosis, Arctic type

HSPD1 APP


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
HSPD1
(0.78)
APP



Citations in the biomedical literature:


Autosomal dominant spastic paraplegia type 13
HSPD1
Hereditary cerebral hemorrhage with amyloidosis, Arctic type
APP



Autosomal dominant spastic paraplegia type 13
Hereditary cerebral hemorrhage with amyloidosis, Arctic type

Synonym(s):
- SPG13

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):
- Diseases of the nervous system -
Classification (ICD10):
(no data available)

Epidemiological data:
Class of prevalence: <1 / 1 000 000
Average age onset: -
Average age of death: -
Type of inheritance: autosomal dominant
Epidemiological data:
(no data available)

External references:
1 OMIM reference -
1 MeSH reference: C537485
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 spastic paraplegia type 13

(no data available)