Disorders


 

Tooth Agenesis, Selective, 1


Synonym(s): Absence of Second Premolars and Third Molars, HYD1, Hypodontia, Autosomal Dominant, Hypodontia/Oligodontia 1, STHAG1

 

OMIM

GeneLocusProtein
MSX14p16.2Homeobox protein MSX-1

Laboratory Test Method Prenatal Carrier *
Boston Children's Hospital, Genetics Diagnostic Laboratory - Waltham, MA, USA  
Centogene AG, Rare Disease Company - Rostock, Germany  
Connective Tissue Gene Tests - Allentown, PA, USA  
diagenos - Osnabrueck, Germany• Mutation scanning of the entire coding region
  
Klinikum Stuttgart, Institute of Clinical Genetics - Stuttgart, Germany  
Praxis fuer Humangenetik Wien - Vienna, Austria  

* Carrier column is relevant to autosomal recessive and X-linked inheritance; column will be blank when it is not relevant (e.g. autosomal dominant inheritance, microdeletions/duplications) and/or is not offered by the lab.

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