NCOA7

nuclear receptor coactivator 7
OMIM: 609752, Gene2Phenotype

2 panels

Panel Reviews Mode of inheritance Details
2 panels

Green NCOA7 in Mendeliome


Version 1.3050

review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Green
  • Literature
Phenotypes
  • Inherited premature ovarian failure MONDO:0019852, NCOA7-related

Green NCOA7 in Primary Ovarian Insufficiency_Premature Ovarian Failure

Level 3: Gonadal and sex development disorders
Level 2: Endocrine disorders
Version 0.355

review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Green
  • Literature
Phenotypes
  • Inherited premature ovarian failure MONDO:0019852, NCOA7-related