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1 OMIM reference -
1 associated gene
3 signs/symptoms
PROTEIN INTERACTIONS: 2
2 OMIM references -
2 associated genes
No signs/symptoms info
Hereditary cerebral hemorrhage with amyloidosis, Arctic type
X-linked diffuse leiomyomatosis - Alport syndrome

APP COL4A5
COL4A6


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
APP
APP
(0.7)
(0.52)
COL4A6
COL4A5



Citations in the biomedical literature:


Hereditary cerebral hemorrhage with amyloidosis, Arctic type
APP
X-linked diffuse leiomyomatosis - Alport syndrome
COL4A5 COL4A6



Hereditary cerebral hemorrhage with amyloidosis, Arctic type
X-linked diffuse leiomyomatosis - Alport syndrome

Synonym(s):
- HCHWA, Arctic type

Synonym(s):
- Xq22.3 microdeletion syndrome

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

Classification (ICD10):
(no data available)
Classification (ICD10):
- Congenital malformations, deformations and chromosomal abnormalities -

Epidemiological data:
(no data available)
Epidemiological data:
Class of prevalence: 1-9 / 1 000 000
Average age onset: neonatal/infancy
Average age of death: -
Type of inheritance: x-linked dominant

External references:
1 OMIM reference -
No MeSH references
External references:
2 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



X-linked diffuse leiomyomatosis - Alport syndrome

(no data available)