SI

sucrase-isomaltase
OMIM: 609845, Gene2Phenotype

4 panels

Panel Reviews Mode of inheritance Details
4 panels

Green SI in Congenital Diarrhoea


Level 2: Gastroenterological disorders
Version 1.13

review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Victorian Clinical Genetics Services
Phenotypes
  • Sucrase-isomaltase deficiency, congenital, MIM# 222900

Green SI in Mendeliome


Version 1.1891

review BOTH monoallelic and biallelic (but BIALLELIC mutations cause a more SEVERE disease form), autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Expert Review
  • Expert Review Green
  • Victorian Clinical Genetics Services
Phenotypes
  • Sucrase-isomaltase deficiency, congenital #222900

Green SI in Miscellaneous Metabolic Disorders


Level 2: Metabolic disorders
Version 1.46

Component of the following Super Panels:

  • Metabolic Disorders Superpanel
  • Progressive Neurological Conditions
  • review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Green
    • Expert Review
    Phenotypes
    • Sucrase-isomaltase deficiency, congenital, MIM# 222900

    Green SI in BabyScreen+ newborn screening


    Level 2: Screening
    Version 1.113

    review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Green
    • BeginNGS
    Phenotypes
    • Sucrase-isomaltase deficiency, congenital, MIM# 222900
    Tags
    • treatable
    • gastrointestinal