LCT

lactase
OMIM: 603202, ClinGen, DECIPHER

3 panels

Panel Reviews Mode of inheritance Details
3 panels

Green LCT in Congenital Diarrhoea


Level 2: Gastroenterological disorders
Version 2.0

1 review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Victorian Clinical Genetics Services
Phenotypes
  • Lactase deficiency, congenital, MIM# 223000

Green LCT in Mendeliome


Version 2.0

2 reviews BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • NHS GMS
  • Expert Review Green
  • Victorian Clinical Genetics Services
Phenotypes
  • Lactase deficiency, congenital, MIM# 223000

Green LCT in Miscellaneous Metabolic Disorders


Level 2: Metabolic disorders
Version 2.0

1 review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • NHS GMS
Phenotypes
  • Lactase deficiency, congenital MIM#223000
  • Other carbohydrate disorders