Orphanet: Familial papillary thyroid carcinoma with renal papillary neoplasia
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Familial papillary thyroid carcinoma with renal papillary neoplasia

Disease definition

An extremely rare inherited tumor syndrome within the familial nonmedullary thyroid cancer group.

ORPHA:97290

Classification level: Disorder
  • Synonym(s):
    • PTC-RCC
  • Prevalence: -
  • Inheritance: -
  • Age of onset: Elderly
  • ICD-10: C64  C73
  • OMIM: 605642
  • UMLS: C1854104
  • MeSH: -
  • GARD: -
  • MedDRA: -

  A summary on this disease is available in Español (2014) Français (2014) Nederlands (2014)

Detailed information

Guidelines

ERN : produced/endorsed by ERN(s)
FSMR : produced/endorsed by FSMR(s)

Additional information

Further information on this disease

Patient-centred resources for this disease

Research activities on this disease

Specialised Social Services

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