OMIA:001901 : Haplotype with homozygous deficiency, RNASEH2B-related

Categories: Mortality / aging (incl. embryonic lethal)

Possible human homologues (MIM numbers): 610181 (trait) , 610326 (gene)

Links to MONDO diseases: No links.

Cross-species summary: Phenes previously called ‘Abortion due to halplotype ….. ’ or ‘Abortion (embryonic lethality)’ , have been renamed to ‘Haplotype with homozygous deficiency, …’ or a phene name that is descriptive of the phenotype observed in homozygous affected animals [14/1/2022

Species in which this phene is found:
taurine cattle (Bos taurus)

Edit History


  • Created by Frank Nicholas on 04 Jan 2014
  • Changed by Frank Nicholas on 04 Mar 2017
  • Changed by Imke Tammen2 on 25 Sep 2021
  • Changed by Imke Tammen2 on 18 Jan 2022