AMH

anti-Mullerian hormone
OMIM: 600957, Gene2Phenotype

3 panels

Panel Reviews Mode of inheritance Details
3 panels

Green AMH in Differences of Sex Development


Level 2: Dysmorphic and congenital abnormality syndromes
Version 0.293

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

Green AMH in Mendeliome


Version 1.1891

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

Amber AMH 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 insuffiency