In addition to mandatory tests:

• Ectropion / Entropion

  Augen

  These are structural eyelid abnormalities affecting a dog's eyes. In cases of entropion, the eyelid rolls inward, causing the eyelashes or fur to rub painfully against the surface of the eyeball. In ectropion, the eyelid sags or rolls outward, leaving the sensitive inner lining of the eye exposed and unprotected.

  Deep dive+

• Multifocal Retinopathy 1(CMR1)

  Augen

  Multifocal Retinopathy 1 is an inherited eye condition affecting the retina, which is the light-sensitive layer at the back of the eye. It causes small, fluid-filled blisters to form beneath this layer, leading to localized areas of retinal detachment. Despite these structural changes, the overall health of the eye is rarely compromised.

  DNA · Passing: Clear or Carrier

  Deep dive+

• Retinal Dysplasia(RD)

  Augen

  Retinal dysplasia is a congenital condition affecting the eyes, where the retina (the light-sensitive tissue at the back of the eye) does not develop properly during growth in the womb. This abnormal development leads to structural defects like folds or gaps in the retinal layers. Because the retina is responsible for sending visual signals to the brain, these imperfections can impair normal vision.

  Augen

  Deep dive+

• Cervical vertebral compressive myelopathy(CVCM)

  Bewegungsapparat

  Cervical vertebral compressive myelopathy, commonly known as Wobbler syndrome, is a condition affecting the spine where the spinal cord in the neck becomes pinched. This compression is caused by malformed neck vertebrae or slipping discs between the bones. Over time, the constant pressure damages the nerve pathways that carry signals from the brain to the limbs.

  Roentgen

  Deep dive+

• Cerebellar abiotrophy(CA)

  Nervensystem

  Cerebellar abiotrophy is an inherited neurological disorder affecting the brain, specifically the cerebellum, which regulates balance and movement coordination. In affected dogs, the nerve cells in this region prematurely degenerate and die off. This progressive cell loss disrupts the brain's ability to control smooth physical movements.

  DNA

  Deep dive+

• Neuroaxonal dystrophy, RNF170-related(NAD)

  Nervensystem

  This is a severe inherited disorder of the nervous system caused by a genetic mutation. It leads to abnormal swellings along the nerve fibers, which disrupt the transmission of signals between the brain and the rest of the body.

  Deep dive+

• Cystinuria(Cyst-1a)

  Nieren

  Cystinuria is an inherited metabolic disorder affecting the kidneys, where the body fails to reabsorb an amino acid called cystine. Instead of being filtered back into the bloodstream, cystine builds up in the urine. Over time, this high concentration causes the amino acid to crystallize, forming painful stones in the bladder and urinary tract.

  Koerperfluessigkeiten · Passing: Clear or Carrier

  Deep dive+