ADRA2A

adrenoceptor alpha 2A
OMIM: 104210, ClinGen, DECIPHER

3 panels

Panel Reviews Mode of inheritance Details
3 panels

Red ADRA2A in Lipodystrophy_Lipoatrophy


Level 2: Dysmorphic and congenital abnormality syndromes
Version 1.40

1 review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Red
  • Genomics England PanelApp
Phenotypes
  • Lipodystrophy, familial partial, type 8, OMIM #620679

Red ADRA2A in Mendeliome


Version 1.4253

1 review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Red
  • Genomics England PanelApp
  • Genomics England PanelApp
Phenotypes
  • Lipodystrophy, familial partial, type 8, OMIM #620679

Red ADRA2A in Monogenic Diabetes


Level 2: Endocrine disorders
Version 0.202

Component of the following Super Panels:

  • Metabolic Disorders Superpanel
  • 1 review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
    Sources
    • Expert Review Red
    • Genomics England PanelApp
    • Genomics England PanelApp
    Phenotypes
    • Lipodystrophy, familial partial, type 8, OMIM #620679