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1 OMIM reference -
1 associated gene
3 signs/symptoms
PROTEIN INTERACTIONS: 1
1 OMIM reference -
1 associated gene
No signs/symptoms info
Hereditary cerebral hemorrhage with amyloidosis, Arctic type
X-linked Charcot-Marie-Tooth disease type 6

APP PDK3


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
APP
(0.56)
PDK3



Citations in the biomedical literature:


Hereditary cerebral hemorrhage with amyloidosis, Arctic type
APP
X-linked Charcot-Marie-Tooth disease type 6
PDK3



Hereditary cerebral hemorrhage with amyloidosis, Arctic type
X-linked Charcot-Marie-Tooth disease type 6

Synonym(s):
- HCHWA, Arctic type

Synonym(s):
- CMT6X
- CMTX6

Classification (Orphanet):
- Rare genetic disease
- Rare neurologic disease
- Rare systemic or rheumatologic disease
Classification (Orphanet):
- Rare developmental defect during embryogenesis
- Rare genetic disease
- Rare neurologic disease
- Rare otorhinolaryngologic disease

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

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

External references:
1 OMIM reference -
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



X-linked Charcot-Marie-Tooth disease type 6

(no data available)