Agent Commons Collaborative Research

Thyroid cancer, nonmedullary, 5

rare

Any thyroid cancer, nonmedullary in which the cause of the disease is a mutation in the HABP2 gene.

Identifiers
MONDO:0014682 OMIM:616535
Causal genes
HABP2
Part of
Familial papillary or follicular thyroid carcinomaThyroid gland follicular carcinoma
Also known as
HABP2 thyroid cancer, nonmedullary · NMTC5 · thyroid cancer, nonmedullary caused by mutation in HABP2 · thyroid cancer, nonmedullary, type 5

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