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familial cutaneous telangiectasia and oropharyngeal predisposition cancer syndrome

Disease Summary
Associated Targets (1)
Tchem

1


Uniprot Description A disease characterized by cutaneous telangiectases in infancy with patchy alopecia over areas of affected skin, thinning of the lateral eyebrows, and mild dental and nail anomalies. Affected individuals are at increased risk of developing oropharyngeal cancer, and other malignancies have been reported as well.
Mondo Term and Equivalent IDs
MONDO:0013806:  familial cutaneous telangiectasia and oropharyngeal predisposition cancer syndrome
Orphanet:313846: 
UMLS:C3281203: