DIRC3 gene related symptoms and diseases

All the information presented here about the DIRC3 gene and its related diseases, symptoms, and test panels has been aggregated from the following public sources: ORPHANET,NCBIGENE,HGNC,OMIM, Mendelian Rare Disease Search Engine.

Top 5 symptoms and clinical features associated to DIRC3 gene

Symptoms // Phenotype % Cases
Neoplasm Uncommon - Between 30% and 50% cases
Pain Uncommon - Between 30% and 50% cases
Carcinoma Uncommon - Between 30% and 50% cases
Hoarse voice Uncommon - Between 30% and 50% cases
Goiter Uncommon - Between 30% and 50% cases

Other less frequent symptoms and clinical features

Patients with DIRC3 gene alterations may also develop some of the following symptoms and phenotypes:
  • Not very common - Between 30% and 50% cases

  • Oral-pharyngeal dysphagia
  • Colon cancer
  • Thyroiditis
  • Thyroid carcinoma
  • Multinodular goiter
  • Papillary thyroid carcinoma
  • Medullary thyroid carcinoma
  • Follicular thyroid carcinoma

And 2 more phenotypes, you can get all of them using our tools for rare diseases.

Rare diseases associated to DIRC3 gene

Here you will find a list of rare diseases related to the DIRC3. You can also use our tool to get a more accurate diagnosis based on your current symptoms.


DIFFERENTIATED THYROID CARCINOMA

Alternate names

DIFFERENTIATED THYROID CARCINOMA Is also known as well-differentiated thyroid carcinoma, pact, tpc, nonmedullary thyroid carcinoma, papillary, papillary or follicular thyroid carcinoma, papillary carcinoma of thyroid, familial nonmedullary thyroid cancer, papillary, ptc

Description

Differentiated thyroid carcinoma (DTC), also known as papillary or follicular thyroid carcinoma, is a slow-growing malignancy usually presenting in adults as an asymptomatic thyroid mass.

Most common symptoms of DIFFERENTIATED THYROID CARCINOMA

  • Neoplasm
  • Pain
  • Carcinoma
  • Hoarse voice
  • Goiter


More info about DIFFERENTIATED THYROID CARCINOMA

SOURCES: ORPHANET OMIM

HEREDITARY CLEAR CELL RENAL CELL CARCINOMA

Alternate names

HEREDITARY CLEAR CELL RENAL CELL CARCINOMA Is also known as hereditary clear cell renal cell adenocarcinoma

Description

Hereditary clear cell renal cell carcinoma (ccRCC) is a hereditary renal cancer syndrome defined as development of ccRCC in two or more family members without evidence of constitutional chromosome 3 translocation, von Hippel-Lindau disease or other tumor predisposing syndromes associated with ccRCC, such as tuberous sclerosis or Birt-Hogg-Dubbé syndrome.


More info about HEREDITARY CLEAR CELL RENAL CELL CARCINOMA

SOURCES: ORPHANET



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