OMIA:001823 : Haplotype with homozygous deficiency HH2, IFT80-related |
Categories: Mortality / aging (incl. embryonic lethal)
Possible human homologues (MIM numbers): 611177 (gene) , 611263 (trait)
Links to MONDO diseases: No links.
Cross-species summary: This phene was previously called ‘Abortion due to halplotype HH2' and has been renamed to ‘Haplotype with homozygous deficiency-HH2, IFT80-related’.
Species in which this phene is found:
taurine cattle (Bos taurus)
Edit History
- Created by Frank Nicholas on 12 Jun 2013
- Changed by Imke Tammen2 on 12 May 2021
- Changed by Imke Tammen2 on 16 Dec 2021
- Changed by Frank Nicholas on 04 Apr 2022