1. Mendelian
  2. Rare Disease Genes
  3. CDH13

CDH13 gene related symptoms and diseases

All the information presented here about the CDH13 gene and its related diseases, symptoms, and test panels has been aggregated from the following public sources: NCBIGENE,OMIM,HGNC, Mendelian Rare Disease Search Engine.

Table of contents:

Top 5 symptoms and clinical features associated to CDH13 gene

Symptoms // Phenotype % Cases
Dysphagia Very Common - Between 80% and 100% cases
Obesity Very Common - Between 80% and 100% cases
Gastroesophageal reflux Very Common - Between 80% and 100% cases
Feeding difficulties in infancy Very Common - Between 80% and 100% cases
Cough Very Common - Between 80% and 100% cases

Other less frequent symptoms and clinical features

Patients with CDH13 gene alterations may also develop some of the following symptoms and phenotypes:

  • Commonly - More than 50% cases

  • Nausea and vomiting
  • Lymphadenopathy
  • Chest pain
  • Esophagitis
  • Clinodactyly of the 5th toe
  • Barrett esophagus
  • Esophageal ulceration
  • Esophageal carcinoma

Rare diseases associated to CDH13 gene

Here you will find a list of rare diseases related to the CDH13. You can also use our tool to get a more accurate diagnosis based on your current symptoms.


ADENOCARCINOMA OF THE ESOPHAGUS

Alternate names

ADENOCARCINOMA OF THE ESOPHAGUS Is also known as esophageal adenocarcinoma, barrett metaplasia

Description

Esophageal adenocarcinoma (EAC) is a sub-type of esophageal carcinoma (EC; see this term) affecting the glandular cells of the lower esophagus at the junction with the stomach.

Most common symptoms of ADENOCARCINOMA OF THE ESOPHAGUS

  • Dysphagia
  • Obesity
  • Gastroesophageal reflux
  • Feeding difficulties in infancy
  • Cough


More info about ADENOCARCINOMA OF THE ESOPHAGUS

SOURCES: OMIM MESH ORPHANET


Potential gene panels for CDH13 gene

Amyotrophic Lateral Sclerosis and Frontotemporal Dementia Sequencing Panel with CNV Detection Panel

United States.

By PreventionGenetics PreventionGenetics Amyotrophic Lateral Sclerosis and Frontotemporal Dementia Sequencing Panel with CNV Detection that also includes the following genes: SOD1 SQSTM1 TARDBP TBK1 UBQLN2 VAPB VCP OPTN CDH13 TREM2

More info about this panel
United States.

CDH13 Panel

United States.

By Fulgent Genetics Fulgent Genetics

This panel specifically test the CDH13 gene.

More info about this panel
United States.

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