NR0B2

nuclear receptor subfamily 0 group B member 2
OMIM: 604630, Gene2Phenotype

2 panels

Panel Reviews Mode of inheritance Details
2 panels

Red NR0B2 in Mendeliome


Version 1.1902

review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Red
  • Victorian Clinical Genetics Services
Phenotypes
  • Obesity, mild, early-onset, MIM# 601665

Red NR0B2 in Severe early-onset obesity


Level 2: Endocrine disorders
Version 1.10

review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Red
  • Genomics England PanelApp
Phenotypes
  • Obesity, mild, early-onset MIM#601665