Hämophilie B [p]

Order number: PSD575
  • *** Partner laboratory
€65.45

VAT incl.

Application: - Differential diagnosis of coagulation disorders. - Identification of symptom-free, female carrier animals The test is performed in a partner laboratory. The mutation investigated in this test is found in the Rhodesian Ridgeback. Other genetic variants are known to be present in Airedale Terrier, Cairn Terrier, Hovawart and Labrador Retriever. Mode of inheritance is X-linked... more
Product information "Hämophilie B [p]"
Application:
- Differential diagnosis of coagulation disorders.
- Identification of symptom-free, female carrier animals
The test is performed in a partner laboratory.
The mutation investigated in this test is found in the Rhodesian Ridgeback. Other genetic variants are known to be present in Airedale Terrier, Cairn Terrier, Hovawart and Labrador Retriever. Mode of inheritance is X-linked recessive.
In the lexicon you will find more information and explanations about the article more
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Animal assignment:
Please enter the name of your animal.
Classification:
Type: DNA tests
Species: Dog
Class: Inherited diseases
Breeding clubs: Deutscher Retriever Club e.V., DRC. DNA-Programm Identität und Eigenschaften
Breed: Mischling Hund, Rhodesian Ridgeback, unbekannt
Group: Blood
A – Locus / Agouti - DOG
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B – Locus (Coat color 'Brown' - DOG)
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Centronuclear Myopathy (CNM)
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crd-PRA
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Curly Coat
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D – Locus (Dilution)
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Cerebellar hypoplasia (Dandy Walker Like...
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E – Locus (Coat color 'Yellow')
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Furnishings
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Glykogen storage disease GSDIIIa
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Golden Retriever PRA 1
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Golden Retriever PRA 2
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Harlequin coat pattern
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L – Locus (hair length)
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K – Locus (dominant black)
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Malignant Hyperthermia - DOG
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Merle coat pattern
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Narcolepsy (Dachshund)
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Narcolepsia (Dobermann)
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Narcolepsy (Labrador)
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Neuronal Ceroid-Lipofuscinosis 1 (Dachshund)
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Neuronal Ceroid-Lipofuscinosis 2 (Dachshund)
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Neuronal Ceroid-Lipofuscinosis 5 (Golden...
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Osteogenesis Imperfecta (Dachshund)
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S – Locus (Piebald)
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Skeletal Dysplasia 2
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Von-Willebrand-Disease Type 1
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Golden Retriever muscular dystrophy
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Cystinuria-A (Newfoundland)
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Cone-rod dystrophy 4 - Progressive Retinal...
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Juvenile Myoclonic Epilepsy
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IVDD-Type 1
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prcd-PRA***
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HNPK
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Exercise Induced Collapse (EIC)***
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Ichtyosis (ICT-A)***
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Collie eye anomaly (CEA)***
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Degenerative Myelopathy (DM)***
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RD_OSD***
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STGD - Stargardt Disease
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Malignant Hyperthermia - HORSE
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Polysaccharide Storage Myopathy 1 (PSSM1***)
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DNA profile Identity DOG (ISAG-22-Marker)
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DNA profile Identity DOG - *** class, extended...
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Neuronal Ceroid Lipofuscinosis 10 (NCL10)
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Em – Locus (melanistic mask)
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Hyperuricosuria
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Hereditary Equine Regional Dermal Asthenia (HERDA)
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Hyperkalemic Periodic Paralysis (HYPP)
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Junctional Epidermolysis Bullosa (JEB)
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Generalized Progressive Retinal Atrophy (gPRA)
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Cone-rod dystrophy 1 (crd-1)
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Myotubular Myopathy (X-linked)
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5 Panel
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Cystinuria II-B
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Ectodermal Dysplasia
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Glycogen Branching Enzyme Deficiency (GBED)
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