Categories: Nervous system phene

Mendelian trait/disorder: unknown

Mode of inheritance: Probably autosomal recessive

Disease-related: yes

Species-specific name: This condition is clinically indistinguishable from daft lamb disease (OMIA 000177-9940 : Cerebellar cortical atrophy in Ovis aries), but differs by the absence of noticeable changes to the cerebellum or other parts of the CNS. In addition to typical congenital neurological clinical science, skeletal fragility and a progressive myopathy was noted.

Breed: Border Leicester (Sheep) (VBO_0001347).
Breeds in which the phene has been documented. (If a likely causal variant has been documented for the phene, see the variant table breeds in which the variant has been reported).