Centronuclear Myopathy (CNM)

Order number: GSD176
€48.79

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Application: a) Carrier identification in offspring after mating of a 'CNM-carrier' with a 'CNM-free' animal, b) Differential diagnosis in cases of clinical muscle insufficiency. Centronuclear Myopathy (CNM), also described as HMLR, or Hereditary Myopathy of Labrador Retrievers, has an autosomal recessive expression. Affected animals show insufficient muscle function resulting in various... more
Product information "Centronuclear Myopathy (CNM)"
Application:
a) Carrier identification in offspring after mating of a 'CNM-carrier' with a 'CNM-free' animal,
b) Differential diagnosis in cases of clinical muscle insufficiency.
Centronuclear Myopathy (CNM), also described as HMLR, or Hereditary Myopathy of Labrador Retrievers, has an autosomal recessive expression. Affected animals show insufficient muscle function resulting in various clinical symptoms.
In the lexicon you will find more information and explanations about the article more
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Classification:
Type: DNA tests
Species: Dog
Class: Inherited diseases
Breeding clubs: Deutscher Retriever Club e.V., DRC. DNA-Programm Identität und Eigenschaften
Breed: Deutsche Dogge, Labrador Retriever, Mischling Hund, Sonstige, unbekannt, verschiedene Rassen
Group: Musculoskeletal system
P1-DRC - Labrador Retriever Bundle A
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Labrador Retriever Bundle B (P3)
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Copper storage tox. Labrador type [p]
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A – Locus / Agouti - DOG
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B – Locus (Coat color 'Brown' - DOG)
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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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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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Neuronal Ceroid-Lipofuscinosis 1 (Dachshund)
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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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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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Collie eye anomaly (CEA)***
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Degenerative Myelopathy (DM)***
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STGD - Stargardt Disease
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Hämophilie B [p]
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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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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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