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Article

Medullary thyroid cancer in a patient with Hirschsprung disease with a C609Y germline RET-mutation.

Journal of pediatric gastroenterology and nutrition - 1 Feb 2005

de Groot Jan Willem B, Sijmons Rolf H, Links Thera P, Plukker John Tn M, Hofstra Robert M W

Abstract excerpt

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Topics

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Share to Carcinoma, Medullary
Share to RET gene
Share to Genetic Predisposition to Disease
Share to Germ-Line Mutation

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Hirschsprung Disease

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Share to Thyroid Neoplasms

Source

Identifiers

PMID: 15699703
DOI: 10.1097/00005176-200502000-00028

Genes

RET

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Medullary thyroid cancer in a patient with Hirschsprung disease with a C609Y germline RET-mutation.PMID 15699703Read ↗

Novel germline RET mutation segregating with papillary thyroid carcinomas.Semantic proximity Read ↗

Thyroid cancer and co-occurring RET mutations in Hirschsprung disease.Semantic proximity Read ↗

Deletion-insertion mutation encompassing RET codon 634 is associated with medullary thyroid carcinoma.Semantic proximity Read ↗

The familial medullary thyroid carcinoma-associated RET E768D mutation in a multiple endocrine neoplasia type 2A case.Semantic proximity Read ↗

The RET E616Q Variant is a Gain of Function Mutation Present in a Family with Features of Multiple Endocrine Neoplasia 2A.Semantic proximity Read ↗

New presentation of familial medullary thyroid carcinoma in 87-year-old patient with high-risk RET proto-oncogene codon 620 mutation.Semantic proximity Read ↗

[Hirschsprung's disease and medullary carcinoma of the thyroids: two diseases in a monogenetic disorder].Semantic proximity Read ↗

Prophylactic thyroidectomy in pediatric carriers of multiple endocrine neoplasia type 2A or familial medullary thyroid carcinoma: mutation in C620 is associated with Hirschsprung's disease.Semantic proximity Read ↗

Hirschsprung's disease and medullary thyroid carcinoma: 15-year experience with molecular genetic screening of the RET proto-oncogene.Semantic proximity Read ↗

A rare variant, I852M, of the RET proto-oncogene in a patient with medullary thyroid carcinoma at age 20 years.Semantic proximity Read ↗

RET receptor signaling: dysfunction in thyroid cancer and Hirschsprung's disease.Semantic proximity Read ↗

ASSOCIATION OF RS2435357 AND RS1800858 POLYMORPHISMS IN RET PROTO-ONCOGENE WITH HIRSCHSPRUNG DISEASE: SYSTEMATIC REVIEW AND META-ANALYSIS.Semantic proximity Read ↗

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