TGFA gene related symptoms and diseases

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

Top 5 symptoms and clinical features associated to TGFA gene

Symptoms // Phenotype % Cases
Micrognathia Very Common - Between 80% and 100% cases
Hypoplasia of the maxilla Very Common - Between 80% and 100% cases
Microdontia Very Common - Between 80% and 100% cases
Abnormality of the face Very Common - Between 80% and 100% cases
Oligodontia Very Common - Between 80% and 100% cases

Other less frequent symptoms and clinical features

Patients with TGFA gene alterations may also develop some of the following symptoms and phenotypes:
  • Commonly - More than 50% cases

  • Abnormality of dental morphology

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Rare diseases associated to TGFA gene

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


Alternate names

OLIGODONTIA Is also known as selective tooth agenesis


Oligodontia is a rare developmental dental anomaly in humans characterized by the absence of six or more teeth.

Most common symptoms of OLIGODONTIA

  • Micrognathia
  • Hypoplasia of the maxilla
  • Microdontia
  • Abnormality of the face
  • Oligodontia

More info about OLIGODONTIA


Potential gene panels for TGFA gene

TGFA Panel

United States.

By Fulgent Genetics Fulgent Genetics

This panel specifically test the TGFA gene.

More info about this panel

Tempus xO assay Panel

United States.

By Tempus Labs, Inc. Tempus xO assay that also includes the following genes: BCL6 RHEB RIPK1 RIPK2 RIPK3 RIT1 BCL7A BCL9 BCR ROBO2

More info about this panel

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