Familial papillary or follicular thyroid carcinoma

rare

A papillary or follicular thyroid gland carcinoma with a genetic component that develops within the same family. Current studies suggest that it is inherited in an autosomal dominant pattern. It is often multifocal and bilateral and usually affects younger patients.

Identifiers: MONDO:0017895 Orphanet:319487
Part of: Differentiated thyroid carcinoma Familial nonmedullary thyroid carcinoma
Also known as: familial nonmedullary thyroid gland carcinoma · familial pure nonmedullary thyroid carcinoma · FNMTC

Subtypes

All diseases Rare only

Disease	ID	Genes
Papillary thyroid Microcarcinoma	MONDO:0011368
Thyroid cancer, nonmedullary, 2	MONDO:0008566
Thyroid cancer, nonmedullary, 3	MONDO:0011653
Thyroid cancer, nonmedullary, 4	MONDO:0014681	FOXE1
Thyroid cancer, nonmedullary, 5	MONDO:0014682	HABP2
Thyroid carcinoma, nonmedullary, with or without cell oxyphilia	MONDO:0011312

Rare disease

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