Cytoscape Web
Click node...

Familial aortic dissection
1 OMIM reference -
1 associated gene
14 connected diseases
No signs/symptoms info
Disease Type of connection
Familial thoracic aortic aneurysm and aortic dissection
Acute myeloid leukemia with abnormal bone marrow eosinophils inv(16)(p13q22) or t(16;16)(p13;q22)
APC-related attenuated familial adenomatous polyposis
Congenital glaucoma
Desmoid tumor
Familial adenomatous polyposis due to 5q22.2 microdeletion
Fanconi anemia
Gardner syndrome
Juvenile glaucoma
Turcot syndrome with polyposis
Moyamoya disease
Baraitser-Winter syndrome
Developmental malformations - deafness - dystonia
Familial idiopathic steroid-resistant nephrotic syndrome with focal segmental hyalinosis
Synonym(s):
- Annuloaortic ectasia
- Cystic medial necrosis of aorta
- Erdheim disease
Classification (Orphanet):
- Rare circulatory system disease
- Rare genetic disease
Classification (ICD10):
- Diseases of the circulatory system -
Epidemiological data:
(no data available)
External references:
1 OMIM reference -
No MeSH references
Gene symbol UniProt reference OMIM reference
MYH11 P35749160745
No signs/symptoms info available.