Disorders


 

Tryptophan Hydroxylase Deficiency


 

OMIM

GeneLocusProtein
TPH212q15Tryptophan 5-hydroxylase 2

Laboratory Test Method Prenatal Carrier *
Medical Neurogenetics - Atlanta, GA, 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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