NR3C2-related disease

Type

Disease
Gene
- NR3C2 / Nuclear Receptor Subfamily 3 Group C Member 2
  4q31.1
  OMIM
  GnomAD
  Ensembl
  HGNC
  VMH
  LOVD
Gene product
- Mineralocorticoid receptor
Disease group(s)
- 24.2 Disorders of steroid metabolism
Child entries
- Mineralocorticoid receptor deficiency
- Mineralocorticoid receptor superactivity