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ASH NO. 234643 AQUA NO. FS25615 GREY STALLION HERD N/N 15HHDESTINED TO BE A2024 BREEDING SEASONAPPLICATION FORM BREEDER DETAILS: Name: ___ Address:___ ABN: ___ Association / Society Membership No:___ Email:___
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01
Obtain the hereditary equine regional dermal form from your veterinarian or relevant authority.
02
Fill in the basic information about the horse, including name, breed, and age.
03
Provide the owner's details, including name, address, and contact information.
04
Include any relevant medical history of the horse, focusing on skin conditions if applicable.
05
Attach any required documentation, such as previous veterinary reports or genetic testing results.
06
Review the completed form for accuracy and completeness.
07
Submit the form to the appropriate regulatory body or your vet's office according to their guidelines.

Who needs hereditary equine regional dermal?

01
Horse breeders who want to assess genetic risks.
02
Veterinarians needing detailed skin condition histories.
03
Equine researchers studying hereditary skin diseases.
04
Horse owners curious about their horse's genetic makeup.
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Hereditary equine regional dermal (HERDA) is a genetic disorder affecting the skin of horses, particularly affecting their dermis. It leads to separation of the skin layers, resulting in lesions and impaired healing.
Breeders and owners of horses diagnosed with HERDA are required to file documentation related to the condition to ensure proper tracking and management of the genetic disorder.
To fill out the HERDA documentation, provide detailed information about the horse, including its lineage, any medical history related to the condition, and any previous assessments conducted by veterinarians.
The purpose of HERDA documentation is to monitor genetic health, inform breeding decisions, and maintain transparency in horse breeding practices, thus preventing the propagation of this disorder.
Information required includes the horse's identification details, owner information, medical records regarding HERDA, and lineage data to track familial occurrences of the disorder.
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