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Hairless - Ectodermal dysplasia (CED Dog)

Hairlessness (ectodermal dysplasia) results in bald (hairless) patches all over the body. The trait occurs in a few breeds, e.g. Chinese Crested Dog and Mexican Naked Dog. It is homozygous lethal. Dogs with two copies of the mutated gene die before birth.

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Harlequin (Coat colour H-Locus Dog)

Harlequin dogs show black patches on a white base coat. It is a modified version of the Merle colouration. This means that all dogs showing the Harlequin pattern in the phenotype also have one copy of the Merle mutation. Dogs without the mutation for Merle (m/m), can be carriers for Harlequin.

The colour is caused by the H allele of the H locus. Homozygous animals (H/H) die before birth.

 

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Hereditary Equine Regional Dermal Asthenia (HERDA Horse)

Hereditary Equine Regional Dermal Asthenia (HERDA) is caused by the presence of abnormal collagen in the skin. This results in skin detachment, severe lesions, ulcerations and wound healing problems.

The disease occurs in the Quarter Horse and related breeds. It is inherited autosomal recessively.

Synonym: Ehlers-Danlos syndrome, hyperelastosis cutis

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Hereditary Nasal Parakeratosis (HNPK Dog)

Hereditary Nasal Parakeratosis (HNPK) is a differentiation disorder of the skin cells (keratinocytes) in the area of the dog's nose. Affected dogs show firm scabs on the upper nose leather and thus a risk of cracks and fissures on the nose.

The pre-damaged skin can be more easily infected by pathogens, which can lead to complications. The animals are otherwise healthy.
The disease occurs in the Labrador Retriever. The inheritance is autosomal recessive.

 

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Also in the Labrador Retriever A package (DRC P1)

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Hoof Wall Separation Disease (HWSD Horse)

Hoof Wall Separation Disease (HWSD) is characterized by a receding dorsal hoof wall. Affected animals have brittle hooves and, depending on the severity of the symptoms, often show lameness or even have to be euthanized.

The disease occurs in Connemara ponies and is inherited autosomal recessively.

 

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Hydrocephalus (HCP Horse)

In hydrocephalus, cerebrospinal fluid accumulation in the brain leads to enlarged skull and death of the foal. The disease occurs in Friesian horses and is inherited autosomal recessively.

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Hyperkalemic Periodic Paralysis (HYPP Horse)

Hyperkalemic Periodic Paralysis (HYPP) is caused by a malformed channel protein in skeletal muscle cells and results in temporary paralysis due to malfunctioning signal transmission from the brain to the muscles/organs.

The disease occurs in the Quarter Horse and related breeds. The inheritance is incomplete autosomal dominant.

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Hyperuricosuria and Hyperuricemia (HUU Dog)

In Hyperuricosuria and Hyperuricaemia (HUU), dogs excrete uric acid instead of allantoin in their urine. This causes increased formation of urinary stones, which can lead to problems.

The disease occurs in many breeds. It is inherited autosomal recessively.

Synonym: Urolithiasis

 

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Ichthyosis (PNPLA1-related Golden Retriever)

Ichthyosis (PNPLA1-related) is a cornification disorder of the skin. This leads to defects in the development of the outer layer of the epidermis. Affected animals show increased scaling (desquamation) and detachment of the outer skin layer.

The hereditary disease occurs in the Golden Retriever. The inheritance is autosomal recessive.

Synonym: ICT-A

 

Genetic Test: available in Shop

Also in the Golden Retriever A package (DRC P2)

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Immune-Mediated Myositis (IMM Horse)

Immune-mediated myositis (IMM) is an immune reaction against the horse's own muscle cells, resulting in muscle loss, often triggered by infections or vaccinations.

The disease occurs in the Quarter Horse and related breeds. The inheritance is incomplete autosomal dominant.

Synonym: MYH1 myopathy

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