- CA – Cerebellar Abiotrophy (CA)
- Dwarfism (Friesian Type)
- Foal Immunodeficiency Syndrome (FIS)
- Glycogen Branching Enzyme Deficiency (GBED)
- Hereditary Equine Regional Dermal Asthenia (HERDA)
- Hoof Wall Separation Disease
- Hydrocephalus (HCP)
- Hyperkalemic Periodic Paralysis (HYPP)
- Immune Mediated Myopathy (IMM)
- Junctional Epidermolysis Bullosa 1 (JEB1)
- Junctional Epidermolysis Bullosa 2 (JEB2)
- Lavender Foal Syndrome (LFS)
- Malignant Hyperthermia – Horse (MH)
- Naked Foal Syndrome (NFS)
- Occipitoatlantoaxial Malformation (OAAM1)
- Polysaccharide Storage Myopathy – Type 1 (PSSM1)
- Severe Combined Immunodeficiency (SCID)
- Squamous Cell Carcinoma (SCC)
- Warmblood Fragile Foal Syndrome (WFFS)