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Golden Retriever Genetic Health Test Panels * :
Golden Retriever Essential Panel:
- Ichthyosis (Golden Retriever Type 1)
- Ichthyosis (Golden Retriever Type 2)
(Aliases: Nonepidermolytic ichthyosis, ICH2, NI)
- Neuronal Ceroid Lipofuscinosis 5 (Golden Retriever Type)
(Aliases: Amaurotic Idiocy, Batten Disease, NCL, NCL5)
- Progressive Retinal Atropy, Golden Retriever 1
(Aliases: GR-PRA1, GR1-PRA)
- Progressive Retinal Atropy, Golden Retriever 2
(Aliases: GR-PRA2, GR2-PRA)
- Progressive Retinal Atropy, Progressive Rod-Cone Degeneration
(Aliases: PRA-PRCD, PRCD)
Golden Retriever Supplemental Panel:
- Degenerative Myelopathy
(Aliases: Canine Degenerative myelopathy, DM)
- Dystrophic Epidermolysis Bullosa (Golden Retriever Type)
(Aliases: Recessive dystrophic epidermolysis bullosa, DEB, EB, RDEB)
- Exercise-Induced Collapse
(Aliases: EIC)
- Muscular Dystrophy (Golden Retriever Type)
(Aliases: Duchenne-type muscular dystrophy, Dystrophin muscular dystrophy, DMD, GRMD)
- Osteogenesis Imperfecta (Golden Retriever Type)
(Aliases: Brittle bone disease, OI)
- Sensory Ataxic Neuropathy
(Aliases: SAN)
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Goldendoodle Genetic Health Test Panels * :
Goldendoodle Essential Panel:
- Congenital Methemoglobinemia
(Aliases: Familial Congennital Methemoglobinemia)
- Degenerative Myelopathy
(Aliases: Canine Degenerative myelopathy, DM)
- Icthyosis (Golden Retriever Type 1)
- Icthyosis (Golden Retriever Type 2)
(Aliases: Nonepidermolytic ichthyosis, ICH2, NI)
- Neonatal Encephalopathy with Seizures
(Aliases: NEWS)
- Neuronal Ceroid Lipofuscinosis 5 (Golden Retriever Type)
(Aliases: Amaurotic Idiocy Batten Disease, NCL, NCL5)
- Osteochondrodysplasia
(Aliases: Skeletal dwarfism, OCD)
- Progressive Retinal Atropy, Golden Retriever 1
(Aliases: GR-PRA1, GR1-PRA)
- Progressive Retinal Atropy, Golden Retriever 2
(Aliases: GR-PRA2, GR2-PRA)
- Progressive Retinal Atropy, Progressive Rod-Cone Degeneration
(Aliases: PRA-PRCD, PRCD)
- Progressive Retinal Atropy, Rod-Cone Dysplasia 4
(Aliases: PRA-rcd4)
- Von Willebrand Disease I
(Aliases: Pseudohemophilia, Vascular hemophilia, von Willebrand disease type 1, von Willebrand's disease, VWDI)
Goldendoodle Supplemental Panel:
- Hereditary Cataracts
(Aliases: Early onset cataracts, Juvenile cataracts, HC, JC)
- Multidrug Resistance 1
(Aliases: Invermectin sensitivity, MDR1 gene defect, Multidrug sensitivity, MDR1)
Goldendoodle Additional Disease Tests:
- Chondrodystrophy (CDDY and IVDD Risk) with or without Chondrodysplasia
(At this time there does not appear to be any association with the CDDY Gene and IVDD disease in Goldendoodles)
(Aliases: CDDY with IVDD, CDPA, Hansen's Type I IVDD, Intervertebral Disc Disease)
- Dystrophic Epidermolysis Bullosa
(Aliases: Recessive dystrophic epidermolysis bullosa, DEB, EB, RDEB)
- Exercise-Induced Collalpse
(Aliases: EIC)
- GM2 Gangliosidosis (Poodle Type)
(Aliases: Sandhoff disease, Type 0 gangliosidosis)
- Muscular Dystrophy (Golden Retriever Type)
(Aliases: Duchenne-type muscular dystrophy, Dystrophin muscular dystrophy, DMD, GRMD)
- Osteogenesis Imperfecta (Golden Retriever Type)
(Aliases: Brittle bone disease, OI)
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Australian Labradoodle Genetic Health Test Panels * :
Australian Labradoodle Essential Panel:
- Degenerative Myelopathy
(Aliases: Canine Degenerative myelopathy, DM)
- Exercise-Induced Collalpse
(Aliases: EIC)
- Hereditary Nasal Parakeratosis
(Aliases: HNPK)
- Neonatal Encephalopathy with Seizures
(Aliases: NEWS)
- Progressive Retinal Atropy, Progressive Cone-Rod Dystrophy 4
(Aliases: Progressive retinal atrophy) - Progressive Retinal Atropy, Progressive Rod-Cone Degeneration
(Aliases: PRA-PRCD, PRCD)
- Von Willebrand Disease I
(Aliases: Pseudohemophilia, Vascular hemophilia, von Willebrand disease type 1, von Willebrand's disease, VWDI)
Australian Labradoodle Supplemental Panel:
- Centronuclear Myopathy
(Aliases: Hereditary myopathy of the Labrador Retriever, Type II muscle fiber deficiency, CNM)
- Cystinuria (Labrador Retriever Type)
(Aliases: Type IA cystinuria)
- Familial Nephropathy (Cocker Spaniel Type)
(Aliases: Brittle bone disease, OI)
- Glycogen Storage Disease VII, PFK Deficiency
(Aliases: Phosphofructokinase deficiency, GSD VII, PFK deficiency)
- Myotubular Myopathy 1
(Aliases: X-linked myotubular myopathy, MTM1, XLMTM)
- Narcolepsy (Labrador Retriever Type)
(Aliases: Brittle bone disease, OI)
- Retinal Dysplasia/Oculoskeletal Dysplasia 1
(Aliases: Dwarfism with retinal dysplasia 1, Inherited retinal dysplasia, Oculoskeletal dysplasia 1, Retinal dysplasia, DRD1, OSD1, RD, RD/OSD)
- Skeletal Dysplasia 2
(Aliases: Dwarfism, SD2)
Australian Labradoodle Additional Disease Tests:
- Congenital Myasthenic Syndrome (Labrador Retriever Type)
(Aliases: CMS)
- Elliptocytosis
- GM2 Gangliosidosis (Poodle Type)
(Aliases: Sandhoff disease, Type 0 gangliosidosis)
- Hyperuricosuria
(Aliases: Urolithiasis, HUU)
- Osteochondrodysplasia
(Aliases: Skeletal dwarfism, OCD)
- Progressive Retinal Atrophy, Golden Retriever 2
(Aliases: GR-PRA2, GR2-PRA)
- Pyruvate Kinase Deficiency (Labrador Retriever Type)
(Aliases: Pyruvate kinase deficiency of erythrocytes, PK deficiency)
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*These panels are from Paw Print Genetics
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