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tumor predisposition syndrome 3 | RareConnect | RareConnect.io

/susceptibility to familial cutaneous melanoma

/glioma susceptibility

/tumor predisposition syndrome 3

tumor predisposition syndrome 3

Rare Disease

MONDO:0014368

Also Known As

CMM10GLM9POT1 tumor predispositionPOT1-TPDPOT1-related tumor predisposition syndromeglioma susceptibility 9glioma susceptibility type 9malignant glioma caused by mutation in POT1melanoma, cutaneous malignant, susceptibility to, 10melanoma, cutaneous malignant, susceptibility to, type 10

Definition

Any hereditary cancer predisposition due to variation(s) in the POT1 gene, which confers a predisposition to development of various types of benign and malignant neoplasms.

Patient-Friendly Information

Comprehensive, easy-to-understand information about this condition

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Associated Genes

Gene data from MyGene.info • Click to view on NCBI Gene

External Resources

OMIM

OMIM:615848 ↗OMIM:616568 ↗

GARD

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