Koirien geeneettiset sairaudet
Valitse koira niin saat listan kaikista Labogenin koirille tarjolla olevista geenettisten sairauksien testeistä. Sairauden nimeä klikkaamalla näet lyhyen kuvauksen sairaudesta, listan roduista joille testi on saatavilla, sairauden periytyvyystiedot, sekä testin käsittelyajan.
Koirien geeneettiset sairaudet
- A
- Acatalasemia
- Achromatopsia (day blindness) (ACHM-1)
- Acral Mutilation Syndrome (AMS)
- Acute respiratory distress syndrome
- Afibrinogenemia (AFG)
- Alaskan Husky enzephalopathy (AHE)
- Alaskan Malamute polyneuropathy (AMPN)
- Alexander disease
- Amelogenesis imperfecta (AI)
- B
- Behaviour propensity
- Brachyuria (stumpy tail)
- Bunny Hopping Syndrome (BHS1)
- C
- C3 deficiency (C3)
- Canine leucocyte adhesion deficiency (CLAD)
- Canine multi-focal retinopathy (CMR1/2/3)
- Canine Multiple System Degeneration (CMSD)
- Cardiomyopathy with juvenile mortality (CJM)
- Cerebellar ataxia (CA)**
- Cerebellar ataxia (CA1)
- Cerebellar deg. and myositis complex (CDMC)
- Cerebellar hypoplasia (CH)
- Cerebral dysfunction (CDFS)
- Charcot-Marie-Tooth Neuropathy (CMT)
- Chondrodysplasia (dwarfism)
- Chondrodysplasia and -dystrophy (CDDY and IVDD risk)
- Cleft lip/palate and syndactyly (CLPS)
- CNS atrophy with cerebellar ataxia (CACA)
- Collie eye anomaly (CEA) partnerlaboratory**
- Color dilution and neurological defects (CDN)
- Combination American Bully
- Combination American Staffordshire Terrier
- Combination Australian Cattle Dog
- Combination Australian Shepherd
- Combination Barbet
- Combination Basenji
- Combination Beagle
- Combination Belgian Shepherd & Dutch Shepherd
- Combination Bernese Mountain Dog
- Combination Black Russian Terrier
- Combination Bolonka Zwetna
- Combination Border Collie
- Combination Bull Mastiff
- Combination Bull Terrier
- Combination Bulldog
- Combination Cairn Terrier
- Combination Cavalier King Charles Spaniel 2
- Combination Cavelier King Charles Spaniel 1
- Combination Chesapeake Bay Retriever
- Combination Chihuahua
- Combination Chinese Crested Dog
- Combination Cocker Spaniel
- Combination Collie
- Combination Continental Toy Spaniel
- Combination Curly Coated Retriever
- Combination Dachshund
- Combination Dachshund 2
- Combination DM exon 2 + MDR1
- Combination Dobermann
- Combination English Springer Spaniel
- Combination Finnish Lapphund
- Combination Fox Terrier
- Combination French Bulldog
- Combination German Shepherd and Wolfdog
- Combination German Shorthaired Pointer
- Combination Giant Schnauzer
- Combination Golden Retriever
- Combination Gordon Setter
- Combination Great Dane
- Combination Great Swiss Mountain Dog
- Combination Havanese
- Combination Heideterrier
- Combination Irish (Red and White) Setter
- Combination Irish Soft-Coated Wheaten Terrier
- Combination Kromfohrländer
- Combination Labradoodle
- Combination Labrador1
- Combination Labrador2
- Combination Lagotto Romagnolo
- Combination Landseer
- Combination Leonberger
- Combination Manchester und Toy Terrier
- Combination Miniature Schnauzer
- Combination Nova Scotia Duck Tolling Retriever
- Combination Old English Sheepdog
- Combination Pomeranian
- Combination Poodle
- Combination Poodle 2
- Combination Portuguese Water Dog
- Combination Pug Dog
- Combination Rhodesian Ridgeback
- Combination Rottweiler
- Combination Russell Terrier 1
- Combination Russell Terrier 2
- Combination Samojede
- Combination Shetland Sheepdog
- Combination Shiba Inu
- Combination Shih Tzu
- Combination Spanish Waterdog
- Combination Tibetan Terrier
- Combination Vizsla
- Combination Weimaraner
- Combination Welsh Corgi
- Combination White Swiss Shepherd
- Combination Yorshire Terrier
- Cone Degeneration (CD)
- Congenital hypothyroidism with goiter (CHG)
- Congenital ichtyosis
- Congenital idiopathic megaesophagus (CIM)
- Congenital myasthenic syndrome (CMS)
- Congenital stationary night blindness (CSNB)
- Copper Toxicosis***
- Copper toxicosis (CT)
- Craniomandibular osteopathy (CMO)
- Cystinuria
- D
- Dandy-Walker-like malformation (DWLM)
- Degenerative myelopathy exon 1 (DM exon1)
- Degenerative myelopathy exon 2 (DM exon2)
- Delayed postoperative haemorrhage (DEPOH)
- Dental-skeletal-retinal anomaly (DSRA)
- Dermatomyositis (DMS)
- Digital hyperkeratosis (DH/HFH)
- Dilatative Kardiomyopathie (DCM)
- Dilated cardiomyopathy (DCM)
- Dilated cardiomyopathy (DCM)
- Disproportionierter Zwergwuchs
- Dry eye curly coat syndrome (CCS)
- Dwarfism (pituitary form)
- Dwarfism (Skeletal dysplasia 2)(SD2)
- Dyserythropoietic anemia and myopathy (DAMS)
- Dystrophic Epidermolysis bullosa (DEB)
- E
- Ectodermal dysplasia/Skin fragility syndrome
- Epidermolytic hyperkeratosis (EHK)
- Episodic falling (EF)
- Exercise induced collapse (EIC)
- Exfoliativer kutaner Lupus erythematodes (ECLE)
- F
- Factor VII deficiency
- Factor XI Deficiency
- Familial nephropathy (FN)
- Familial Nephropathy (FN) partnerlaboratory***
- Familial thyroid follicular cell carcinoma (FZFC)
- Fanconi syndrome
- Finnish Hound ataxia (FHA)
- Fucosidosis
- G
- Gallbladder mucoceles
- Glanzmann thrombasthenia (GT)
- Glaucoma and Goniodysgenesis (GG)
- Globoid cell leucodystrophy (Krabbe-disease)
- Glycogen sorage disease GSD Ia
- Glycogen storage disease GSD II (Pompe)
- Glycogen storage disease type IIIa (GSD3a)
- GM1-Gangliosidosis (GM1)
- GM2-gangliosidosis (Sandhoff disease)(GM2)
- Grey Collie syndrome (GCS)
- H
- Haemophilia A (factor VIII deficiency)
- Hair shaft dystrophy (HSD)
- Hemophilia A (factor VIII deficiency)
- Hemophilia B (factor IX deficiency)
- Hemorrhagic diathesis (Scott syndrom)
- Hereditary ataxia (HA)
- Hereditary Cataract (HSF4)***
- Hereditary catract (HSF4)
- Hereditary Deafness (DINGS1&2)
- Hereditary Deafness (EOAD)
- Hereditary myopathy (CNM)
- Hereditary nasal parakeratosis (HNPK)
- Hereditary neuropathy (GHN)
- Hereditäre nasale Parakeratose (HNPK)
- Hyperuricosuria (SLC)
- Hypomyelination/Shaking puppy syndrome (SPS)
- Hypophosphatasie (HPP)
- I
- Ichthyosis
- Ichthyosis type 2
- Ichthyosis****
- Imerslund-Gräsbeck syndrome (IGS)
- Inflammatory myopathy
- Inflammatory pulmonary disease (IPD)
- J
- Junctional epidermolysis bullosa (JEB)
- Juvenile Enzephalopathie (JBD)
- Juvenile epilepsy (JE)
- Juvenile laryngeal paralysis & polyneuropathy (JLPP)
- Juvenile myoclonic epilepsy (JME)
- L
- L-2-hydroxyglutaric aciduria (L2HGA)
- Lafora disease
- Lagotto storage disease (LSD)
- Laryngeal paralysis
- Laryngeal paralysis with polyneuropathy type 3 (LPPN3)
- Late onset ataxia (LOA)
- Leonberger polyneuropathy (LPN1)
- Leonberger Polyneuropathy 2 (LPN2)
- Lethal acrodermatitis (LAD)
- Lethal lung disease (LAMP3)
- Leukocyte adhesion deficiency type III (LAD3)
- Leukoencephalomyelopathy (LEMP)
- Leukoencephalopathy (LEP)
- LimbÄGirdle Muscular Dystrophy (LGMD)
- Lundehund syndrome
- Lysosomal storage disease (LSD)
- M
- Macrothrombocytopenia (MTC)
- Macular corneal dystrophy (MCD)
- Malignant hyperthermia (MH)
- Maxillary canine tooth mesioversion (MCM)
- May-Hegglin anomaly (MHA)
- MCAD deficiency
- MDR1 gene variant-Ivermectin hypersensibility
- MERTK-PRA
- Methaemoglobinaemia (MetHg)
- Microphthalmia (RBP4)
- Mitochondrial fission encephalopathy - PCR
- Mucopolysaccharidosis type IIIa (MPS3a)
- Mucopolysaccharidosis Type IIIb (MPS3B)
- Mucopolysaccharidosis Type VI
- Mucopolysaccharidosis type VII (MPS 7)
- Multiocular defect (MOD)
- Muscular dystrophy (MD)
- Musladin-Lueke syndrome (MLS)
- Mycobacterium avium complex sensitivity (MAC)
- Myostatin mutation (Bully gene)
- Myotonia congenita
- Myxomatous Mitral Valve Disease (MMVD)
- N
- Narcolepsy
- Necrotizing meningoencephalitis (NME/PDE)
- necrotizing myelopathy (HNM)
- Nemalin myopathy
- Neonatal cortical cerebellar abiotrophy (NCCD
- Neonatal encephalopathy with seizures (NEWS)
- Neuroaxonal dystrophy (NAD)
- Neuronal ceroid lipifuscinosis (NCL)
- Neuronal ceroid lipifuscinosis (NCL) partnerlab***
- Neuronal ceroid lipofuscinosis (NCL)
- Nierendysplasie und Leberfibrose (RDHN)
- O
- Obesity
- Osteochondrodysplasia (OCD)
- Osteogenesis imperfecta (brittle bone dis.)
- P
- Paket Continental Bulldog
- Paradoxical pseudomyotonia (PP)
- Paroxysmal Exercixe-Induced Dyskinesia (PED)
- Paroxysomal dyskinesia (PxD)
- Persistent Müllerian duct syndrome (PMDS)
- Phosphofructokinase deficiency (PFKD)
- Polycystic kidney disease (PKD)
- Postoperative hemorrhage (P2Y12)
- PRA with neurodegeneration (PCYT2 deficiency)
- Prekallikrein deficiency (KLK)
- Primary ciliary dyskinesia (PCD)
- Primary hyperoxaluria (PH)
- Primary Immunodeficiency type 2 (PIPS
- Primary lens luxation (PLL)
- Primary open angle glaucoma (POAG)
- Primary open angle glaucoma + lens luxation
- Progressive retina atrophy (rcd3-PRA)
- Progressive Retinaatrophie (BBS2-PRA)
- Progressive Retinaatrophie (domin. Form PRA)
- Progressive Retinaatrophie (IFT122-PRA)
- Progressive Retinaatrophie (rcd1a-PRA)
- Progressive retinal atrophia (crd1-PRA)
- Progressive retinal atrophia (crd2-PRA)
- Progressive retinal atrophia (rcd2-PRA)
- Progressive Retinal Atrophy (Bas-PRA)
- Progressive retinal atrophy (BBS4ÄPRA)
- Progressive retinal atrophy (CNGA1-PRA)
- Progressive retinal atrophy (cord1-PRA)
- Progressive retinal atrophy (crd-PRA)
- Progressive Retinal Atrophy (crd3-PRA)
- Progressive retinal atrophy (g-PRA)
- Progressive retinal atrophy (GR-PRA2)
- Progressive retinal atrophy (GR_PRA1)
- Progressive retinal atrophy (GUCY2DÄPRA)
- Progressive retinal atrophy (JPH2-PRA)
- Progressive Retinal Atrophy (pap-PRA1)
- Progressive Retinal Atrophy (PRA)
- Progressive retinal atrophy (PRA3)
- Progressive Retinal Atrophy (PRA4)
- Progressive retinal atrophy (prcd-PRA)partner***
- Progressive retinal atrophy (rcd1-PRA)
- Progressive retinal atrophy (rcd4-PRA)
- Progressive Retinal Atrophy (Type B1 PRA, HIVEP3
- Progressive retinal atrophy (XL-PRA)
- Progressive retinal atrophy early-onset (eo-PRA)
- Protein losing nephropathy (PLN)
- Pyruvat dehydrogenase phosphatase 1deficiency
- Pyruvate kinase deficiency (PK)
- R
- Raine syndrome
- Renal Cystadenocarcinoma and nodular fibrosis (RCND)
- Retinal dysplasia (OSD) Partnerlaboratory***
- Retinale Dysplasie (OSD)
- Robinow-like-Syndrom (DVL2)
- S
- Sensory neuropathy (SN)
- Severe combined immunodeficiency (SCID)
- Shar Pei Autoinflammatory Disease (SPAID)
- Spinal dysraphism
- Spinocerebellar ataxia (SCA)
- Spondylocostal dysostosis (Comma defect)
- Spongiforme Leukoenzephalomyelopathie (SLEM)**
- Spongy degeneration with cerebellar ataxia 1
- Spongy degeneration with cerebellar ataxia 2
- Squamous cell carcinoma of the toe
- Startle disease
- STGD-PRA (Stargardt)
- Subakute nekrotisierende Enzephalopathie(SNE)
- Succinic semialdehyde dehydrogenase deficiency (SSADHD)
- T
- Thrombopathia
- Trapped neutrophil syndrome (TNS)
- U
- Upper Airway Syndrome (UAS)
- V
- van den Ende-Gupta syndrome (VDEGS)
- Ventrikuläre Arrhythmie (IVA)
- Vitamin D dependent rickets (VDR)
- von Willebrand disease type I (vWD1)
- von-Willebrand disease type II (vWD 2)
- von-Willebrand disease type III (vWD3)
- X
- X-chromosomal severe immuno defiziency
- X-linked myopathy (XL-MTM)
- Xanthinuria type II
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