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Familial abdominal aortic aneurysm
4 OMIM references -
1 associated gene
15 connected diseases
No signs/symptoms info
Disease Type of connection
Acrogeria
Ehlers-Danlos syndrome, vascular type
Familial cerebral saccular aneurysm
Bilateral striopallidodentate calcinosis
Dermatofibrosarcoma protuberans
Familial multiple meningioma
CARASIL
Atelosteogenesis type I
Atelosteogenesis type III
Autosomal dominant Larsen syndrome
Boomerang dysplasia
Congenital glaucoma
Juvenile glaucoma
Spondylocarpotarsal synostosis
Spondyloepimetaphyseal dysplasia - short limb - abnormal calcification
Synonym(s):
(no synonyms)
Classification (Orphanet):
- Rare circulatory system disease
- Rare genetic disease
Classification (ICD10):
- Diseases of the circulatory system -
Epidemiological data:
(no data available)
External references:
4 OMIM references -
No MeSH references
Gene symbol UniProt reference OMIM reference
COL3A1 P02461120180
No signs/symptoms info available.