NEUROG3

neurogenin 3
OMIM: 604882, ClinGen, DECIPHER

7 panels

Panel Reviews Mode of inheritance Details
7 panels

Green NEUROG3 in Congenital Diarrhoea


Level 2: Gastroenterological disorders
Version 1.30

1 review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Victorian Clinical Genetics Services
Phenotypes
  • Diarrhoea 4, malabsorptive, congenital, MIM# 610370

Green NEUROG3 in Mendeliome


Version 1.4851

1 review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Victorian Clinical Genetics Services
Phenotypes
  • Diarrhoea 4, malabsorptive, congenital, MIM# 610370

Green NEUROG3 in Monogenic Diabetes


Level 2: Endocrine disorders
Version 0.224

Component of the following Super Panels:

  • Metabolic Disorders Superpanel
  • 1 review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Green
    • UKGTN
    Phenotypes
    • congenital malabsorptive diarrhea 4 MONDO:0012479

    Green NEUROG3 in Pituitary hormone deficiency

    Level 3: Pituitary disorders
    Level 2: Endocrine disorders
    Version 0.226

    1 review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Green
    • Literature
    • Literature
    Phenotypes
    • Congenital malabsorptive diarrhea 4, MONDO:0012479
    • Hypogonadotropic hypogonadism, MONDO:0018555

    Green NEUROG3 in Additional findings_Paediatric


    Level 2: Screening
    Version 0.280

    1 review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Green
    • BabySeq Category C gene
    Phenotypes
    • Diarrhoea 4, malabsorptive, congenital, MIM# 610370

    Green NEUROG3 in Genomic newborn screening: BabyScreen+


    Level 2: Screening
    Version 1.148

    2 reviews BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Green
    • BabySeq Category C gene
    • BeginNGS
    Phenotypes
    • Diarrhoea 4, malabsorptive, congenital, MIM# 610370
    Tags
    • treatable
    • gastrointestinal

    Green NEUROG3 in Hypogonadotropic hypogonadism

    Level 3: Pituitary disorders
    Level 2: Endocrine disorders
    Version 0.137

    1 review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Green
    • Literature
    Phenotypes
    • Congenital malabsorptive diarrhea 4, MONDO:0012479
    • Hypogonadotropic hypogonadism, MONDO:0018555