Arthrogryposis multiplex congenita, AGRN-related, cattle
MONDO:1012800Any arthrogryposis multiplex congenita that occurs in cattle due to a mutation in the AGRN gene.
Also known as: Bovine Hereditary Arthrogyposis Multiplex Congentia, BHAC, curly calf syndrome
0 clinical trials for this condition and its sub-types.
Follow this condition — get notified about new trialsBroader categories
Disease
(618)
Arthrogryposis multiplex congenita, cattle
(0)
Arthrogryposis multiplex congenita, non-human animal
(0)
Developmental defect during embryogenesis, non-human animal
(0)
Disorder of development or morphogenesis, non-human animal
(0)
Hereditary disease, non-human animal
(0)
Non-human animal disease
(0)
We haven't found any trials for this condition yet. Follow it to get notified when new trials appear.