LHX8

LIM homeobox 8
OMIM: 604425, Gene2Phenotype

2 panels

Panel Reviews Mode of inheritance Details
2 panels

Red LHX8 in Mendeliome


Version 1.1891

review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Literature
Phenotypes
  • Inherited premature ovarian failure, MONDO:0019852, LHX8-related

Green LHX8 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 Green
  • Literature
Phenotypes
  • Primary ovarian insufficiency