Phenotypes for disease #00583 (FCTCS (telangiectasia, cutaneous, and cancer syndrome, familial), OMIM:614564)

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AscendingPhenotype ID     

Phenotype details     

Diagnosis/Initial     

Diagnosis/Definite     

Inheritance     

Age/Examination     

Age/Diagnosis     

Age/Onset     

Phenotype/Onset     

Protein     

Owner     

Individual ID     
0000188409 telangiectases, thinning lateral part eyebrows, patchy alopecia (prominent telangiectases skin), thin dental enamel, dental caries (primary and secondary dentition), oropharyngeal cancer (third decade of life or later) - - Familial, autosomal dominant - - - - - LOVD 00249444
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