Спадкові хвороби Собака
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Спадкові хвороби Собака
- 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 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 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 Swiss Mountain Dog
- 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 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 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 hemorrhage (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)
- 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
- Methemoglobinemia (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
- 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 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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