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1 OMIM reference -
1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 1
1 OMIM reference -
1 associated gene
No signs/symptoms info
Ehlers-Danlos syndrome, cardiac valvular type
Hereditary cerebral hemorrhage with amyloidosis, Flemish type

COL1A2 APP


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
COL1A2
(0.52)
APP



Citations in the biomedical literature:


Ehlers-Danlos syndrome, cardiac valvular type
COL1A2
Hereditary cerebral hemorrhage with amyloidosis, Flemish type
APP



Ehlers-Danlos syndrome, cardiac valvular type
Hereditary cerebral hemorrhage with amyloidosis, Flemish type

Synonym(s):
- EDS, cardiac valvular type

Synonym(s):
- HCHWA, Flemish type

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

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

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

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

No signs/symptoms info available.