AMHR2

anti-Mullerian hormone receptor type 2
OMIM: 600956, Gene2Phenotype

3 panels

Panel Reviews Mode of inheritance Details
3 panels

Green AMHR2 in Differences of Sex Development


Level 2: Dysmorphic and congenital abnormality syndromes
Version 0.293

review Unknown
Sources
  • Victorian Clinical Genetics Services
  • Expert Review Green

Green AMHR2 in Mendeliome


Version 1.1891

review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Victorian Clinical Genetics Services
Phenotypes
  • Persistent Mullerian duct syndrome, type II MIM#261550

Amber AMHR2 in Primary Ovarian Insufficiency_Premature Ovarian Failure

Level 3: Gonadal and sex development disorders
Level 2: Endocrine disorders
Version 0.328

review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Amber
  • Royal Melbourne Hospital
Phenotypes
  • Primary ovarian insufficiency