1. Mendelian
  2. Genes
  3. LINC02478

LINC02478 gene related symptoms and diseases

All the information presented here about the LINC02478 gene and its related diseases, symptoms, and test panels has been aggregated from the following public sources: NCBIGENE,HGNC, Mendelian Rare Disease Search Engine.

Table of contents:

Top 5 symptoms and clinical features associated to LINC02478 gene

Symptoms // Phenotype % Cases
Dental malocclusion Very Common - Between 80% and 100% cases
Hypoplasia of dental enamel Very Common - Between 80% and 100% cases
Open bite Very Common - Between 80% and 100% cases
Amelogenesis imperfecta Very Common - Between 80% and 100% cases
Anterior open bite Very Common - Between 80% and 100% cases

Other less frequent symptoms and clinical features

Patients with LINC02478 gene alterations may also develop some of the following symptoms and phenotypes:

  • Commonly - More than 50% cases

  • Yellow-brown discoloration of the teeth
  • Anterior open-bite malocclusion
  • Dental enamel pits

Rare diseases associated to LINC02478 gene

Here you will find a list of rare diseases related to the LINC02478. You can also use our tool to get a more accurate diagnosis based on your current symptoms.


AMELOGENESIS IMPERFECTA, TYPE IH; AI1H

Description

Amelogenesis imperfecta type IH is characterized by hypoplastic and hypomineralized tooth enamel that may be rough, pitted, and/or discolored (Wang et al., 2014 and Poulter et al., 2014).

Most common symptoms of AMELOGENESIS IMPERFECTA, TYPE IH; AI1H

  • Dental malocclusion
  • Hypoplasia of dental enamel
  • Open bite
  • Amelogenesis imperfecta
  • Anterior open bite


More info about AMELOGENESIS IMPERFECTA, TYPE IH; AI1H

SOURCES: OMIM



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