Disorders


 

Congenital Lactase Deficiency


 

OMIM

GeneLocusProtein
LCT2q21Lactase-phlorizin hydrolase

Laboratory Test Method Prenatal Carrier *
Center for Human Genetics and Laboratory Medicine Martinsried, Molecular Genetics - Martinsried, Germany  
GENETAQ, Molecular Genetics Centre - Malaga, Spain• Targeted mutation analysis
  

* 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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