Table 3.
Hereditary diseases in sheep: genetic mutations and inheritance types.
| Disease / syndrome | Genetic cause/Mutation | Main symptoms | Breeds affected | Inheritance |
|---|---|---|---|---|
| Spider lamb Syndrome | Mutation in FGFR3 gene (codon 700) | Skeletal deformities, long limbs, lethality | Suffolk, Hampshire | Autosomal recessive |
| Entropion | Polygenic, some evidence on chromosome 15 | Inward-turning eyelids, eye irritation | Swiss White Alpine, others | Polygenic |
| Cryptorchidism | Likely polygenic | Undescended testicle(s), infertility | Various | Polygenic |
| Congenital muscular dystrophy | Mutation in LAMA2 gene | Muscle weakness, stunted growth | Texel (rare) | Autosomal recessive |
| Dermatosparaxis (Ehlers-Danlos type) | Mutation in ADAMTS2 gene | Fragile, easily torn skin | White Dorper, Norwegian White | Autosomal recessive |
| Heritable cataracts | Likely associated with ovine chromosome 6 | Clouded lens, impaired vision | Romney, Merino | Likely recessive or dominant |
| β-Mannosidosis | Deficiency of β-mannosidase enzyme | Neurological signs, developmental delay | Nubian goats, some sheep | Autosomal recessive |