Disorders


 

Hyperlysinemia


Synonym(s): Lysine Intolerance

 

OMIM

GeneLocusProtein
AASS7q31.3Alpha-aminoadipic semialdehyde synthase

Laboratory Test Method Prenatal Carrier *
Baylor Research Institute, Institute of Metabolic Disease - Dallas, TX, USA• Analyte
  
Dayton Children's Medical Center, Molecular and Biochemical Genetics Laboratory - Dayton, OH, USA• Analyte
  
Denver Genetic Laboratories, UCD Biochemical Genetics Laboratory - Aurora, CO, USA• Analyte
  
Duke University Health System, Pediatric Biochemical Genetics Lab - Durham, NC, USA• Analyte
  
Medical Neurogenetics - Atlanta, GA, USA• Analyte
  
Oregon Health and Science University, Knight Diagnostic Laboratories - Biochemical Genetics Laboratory - Portland, OR, USA• Analyte
  
Stanford Clinical Laboratories, Biochemical Genetics Laboratory - Palo Alto, CA, USA• Analyte
  
Universidad Autonoma de Madrid, Centro de Diagnostico de Enfermedades Moleculares - Madrid, Spain• Analyte
  
University of California San Diego, Biochemical Genetics Laboratory - La Jolla, CA, USA• Analyte
  
Yale University School of Medicine, Biochemical Disease Detection Laboratory - New Haven, CT, USA• Analyte
  

* 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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