OMIA:001888 : Muscular dystrophy, Becker type |
Categories: Muscle phene
Possible human homologues (MIM numbers): 300376 (trait) , 300377 (gene)
Links to relevant human diseases in MONDO:
Cross-species summary: Variants in the DMD gene may give rise to phenotypes with different severity. True null alleles cause the more severe Duchenne muscular dystrophy (OMIA:001081), while alleles with partial remaining protein function give rise to the milder Becker muscular dystrophy.
Species in which this phene is found:
dog (Canis lupus familiaris)
domestic cat (Felis catus)
pig (Sus scrofa)
Edit History
- Created by Frank Nicholas on 06 Nov 2013
- Changed by Imke Tammen2 on 27 Oct 2022
- Changed by Imke Tammen2 on 22 Feb 2023
- Changed by Imke Tammen2 on 27 Feb 2023
- Changed by Imke Tammen2 on 25 Mar 2023
- Changed by Imke Tammen2 on 04 Mar 2024