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MIM:614564 - CUTANEOUS TELANGIECTASIA AND CANCER SYNDROME, FAMILIAL; FCTCS
Xenbase Genes: atr
Human Disease Resource: MIM
MONDO:0013806 - familial cutaneous telangiectasia and oropharyngeal predisposition cancer syndrome |
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MONDO:0013806 - familial cutaneous telangiectasia and oropharyngeal predisposition cancer syndrome |