RHOXF1

Rhox homeobox family member 1
OMIM: 300446, ClinGen, DECIPHER

2 panels

Panel Reviews Mode of inheritance Details
2 panels

Amber RHOXF1 in Mendeliome


Version 2.362

3 reviews X-LINKED: hemizygous mutation in males, biallelic mutations in females
Sources
  • Expert Review Amber
  • Literature
Phenotypes
  • Spermatogenic failure, MONDO:0004983, RHOXF1-related

Amber RHOXF1 in Infertility and Recurrent Pregnancy Loss


Version 2.38

3 reviews X-LINKED: hemizygous mutation in males, biallelic mutations in females
Sources
  • Expert Review Amber
  • Literature
  • Literature
Phenotypes
  • Spermatogenic failure, MONDO:0004983, RHOXF1-related