NEUROG3

neurogenin 3
OMIM: 604882, ClinGen, DECIPHER

5 panels

Panel Reviews Mode of inheritance Details
5 panels

Green NEUROG3 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
  • Diarrhoea 4, malabsorptive, congenital, MIM# 610370

Green NEUROG3 in Mendeliome


Version 2.0

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 1.0

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

Green NEUROG3 in Additional findings_Paediatric


Level 2: Screening
Version 1.0

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 2.0

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