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Familial abdominal aortic aneurysm
4 OMIM references -
1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 1
Spondyloepimetaphyseal dysplasia - short limb - abnormal calcification
1 OMIM reference -
1 associated gene
No signs/symptoms info
Familial abdominal aortic aneurysm
Spondyloepimetaphyseal dysplasia - short limb - abnormal calcification

COL3A1
(UniProt - OMIM)
 DDR2
(UniProt - OMIM)

INTERACTOME
ASSOCIATIONS
(click on a score value to see the evidence)
COL3A1
(0.52)
DDR2


Citations in the biomedical literature:


Familial abdominal aortic aneurysm
COL3A1
Spondyloepimetaphyseal dysplasia - short limb - abnormal calcification
DDR2



Familial abdominal aortic aneurysm
Spondyloepimetaphyseal dysplasia - short limb - abnormal calcification

Classification (Orphanet):
- Rare circulatory system disease
- Rare genetic disease
Classification (Orphanet):
- Rare bone disease
- Rare developmental defect during embryogenesis
- Rare genetic disease
Classification (ICD10):
- Diseases of the circulatory system -
Classification (ICD10):
- Congenital malformations, deformations and chromosomal abnormalities -
Epidemiological data:
(no data available)
Epidemiological data:
Class of prevalence: -
Average age onset: -
Average age of death: -
Type of inheritance: autosomal recessive
External references:
4 OMIM references -
No MeSH references
External references:
1 OMIM reference -
No MeSH references
No signs/symptoms info available.