Rhodesian Ridgeback PANEL
RIDGE, JME, DM, MH, DLOK, BLOK, HEMB, EOAD
RR-PANEL
Complete package of genetic tests for prevention of genetic health in Rhodesian Ridgebacks.
Rhodesian Ridgeback PANEL + RRIVA
RIDGE, JME, DM, MH, DLOK, BLOK, HEMB, EOAD, RRIVA
RR-PANEL+RRIVA
Complete package of genetic tests for prevention of genetic health in Rhodesian Ridgebacks, including genetic test for Inherited Ventricular Arrhythmia (RRIVA).
English Bulldog PANEL
MH, DM, HUU, CMR1, CYST, DVL2
AB-PANEL
A complete package of genetic tests for the prevention of genetic health in Dalmatian breed. The package includes genetic tests...
Dalmatian PANEL
MH, DM, ARDS, HUU, BLOK, ELOK
DA-PANEL
A complete package of genetic tests for the prevention of genetic health in Dalmatian breed. The package includes genetic tests...
Early Adult Onset Deafness in Border Collies
deafness, hearing loss
EAOD
Early Adult Onset Deafness (Border Collie type) is a condition characterised by a gradual deterioration of hearing in adult Border Collies. Hearing loss or impairment occurs at around 3-5 years of age and is manifested by a reduced distance at which the individual responds to acoustic stimuli.
Border Collie PANEL
MH, DM, MDR1, CEA, GGD, IGS, NCL, RS, TNS, RS, EAOD
BOC-PANEL
A complete package of genetic tests for the prevention of genetic health in Border Collies. The package includes genetic tests for: Malignant Hyperthermia (MH) Degenerative Myelopathy (DM) Multiple Drug Resistance (MDR1) Collie Eye Anomalies (CEA) Goniodysgenesis and glaucoma (GGD) Intestinal malabsorption of cobalamin (IGS) Neuronal Ceroid Lipofuscinosis (NCL) Raine Syndrome (RS) Trapped Neutrophil Syndrome (TNS) Sensory Neuropathy (SN) Early Auditory Onset Deafness (EAOD)
German Shepherd PANEL
DM, LLOK, DWARF, MDR1
DS-PANEL
Package of genetic tests for prevention of genetic health in Rhodesian Ridgebacks. The package includes genetic tests: Degenerative myelopathy (DM) Hair Length (Locus L) Dwarfism (DWARF) Multidrug resistance 1 (MDR1)
Poodle PANEL Large
MH, DM, NEWS, PRA-prcd, PRA-rcd4, OCD, VWD I, GM2, BLOK, ELOK
PUDL Panel XL
A complete package of genetic tests for the prevention of genetic health in Poodles. The package is suitable for all types of Poodles (Large, Middle, Miniature, Toy). The package includes genetic tests: MH, DM, NEWS, PRA-prcd, PRA-rcd4, OCD, VWD I, GM2, BLOK, ELOK.
Poodle PANEL Small
DM, PRA-prcd, PRA-rcd4, BLOK, ELOK
PUDL Panel S
Basic package of genetic tests for the prevention of genetic health in poodles. The package is suitable for all types of poodles (Large, Middle, Miniature, Toy). The package includes genetic tests: DM, PRA-prcd, PRA-rcd4, BLOK, ELOK.
Ridge predisposition
Ridge gene test, Ridgelessness, Dermoid Sinus predisposition
RIDGE
The ridge formation in Rhodesian and Thai Ridgeback is caused by mutation (duplication of stretch of DNA sequence including several genes). The mutation is called simply a ridge gene and shows dominant inheritance.
Juvenile Myoclonic Epilepsy
Myoclonic seizures
JME
The disease is characterized by myoclonic seizures, which cause rapid uncontrolled muscle jerks and twitches
Malignant Hyperthermia
Canine stress syndrome
MH
It is a congenital disorder of skeletal muscle which is manifested by the significant increase in temperature (hyperthermia) up to 45°C, accelerated and irregular heart rate (tachycardia and arrhythmia), hyperventilation, muscle rigidity and may result in renal failure and death...
Degenerative Myelopathy
DM
It is a neuromuscular disease causing a gradual muscle weakness on the hindlimb and back, which is manifested by poor coordination of movements, cramped and asymmetric walking, or incontinence.
Early Onset Adult Deafness
Hearing loss
EOAD
The genetic disease that is characterised by hearing loss early in life, in which affected individuals lose their sense of hearing within 1-2 years after birth...
Haemophilia B
Christmas disease, Factor IX deficiency
HEMB
It is a rare blood disorder in which the blood is unable to clot properly, leading to excessive bleeding. Bleeding can be initiated from injury, trauma and surgery.
Inherited Ventricular Arrhythmia (RR IVA)
Arrhythmia, Sudden death
RR IVA
A research team led by Dr Kathryn Meurs described the genetic variant associated with Inherited Ventricular Arrhythmia in Rhodesian Ridgebacks (RR IVA)...
Multidrug resistance 1
Ivermectin sensitivity, MDR1 gene defect, Multidrug sensitivity
MDR1
Multidrug resistance 1 is a hereditary disease that makes affected dogs particularly sensitive to certain drugs...
B-locus
Liver nose, Brown
BLOK
The tested variant causes brown colouring of a nose ("livernose"), mucous membranes and claws. The inheritance is autosomal recessive (black allele and colour is dominant).
D Locus
Dilution, d1 allele
DLOK
The tested variant causes coat colour dilution. In black-coloured individuals of different breeds, the hair appears gray (blue)...
E-Locus
Extension, Yellow, Lemon
ELOK
The E locus determines whether the dog will have yellow pigment only, or whether it can also have one of the other coat colours (brown, black)...
Cone degeneration
Achromatopsia, Day blindness, Hemeralopia, Rod monochromacy, CD1
CD
Cone degeneration (also called Achromatopsia) is a disease characterized by loss of cone photoreceptor function, resulting in daytime blindness...
Hereditary Cataract
Early onset cataracts, Juvenile cataracts
HC
Hereditary cataract (cataract) is a disease affecting the lens of the eye in which the lens gradually becomes cloudy...
Acute respiratory distress syndrome
ARDS
Acute Respiratory Distress Syndrome (ARDS) is an inherited condition in Dalmatians that severely affects the lungs, causing severe respiratory distress and death...
Progressive Retinal Atrophy rcd4
Rod-Cone Dysplasia 4
PRA-RCD4
Progressive Retinal Atrophy rcd4 is an eye disease that is inherited in an autosomal recessive manner. The disease leads to degeneration of retinal photoreceptor cells in dog...
Progressive rod-cone degeneration
Progressive Retinal Atrophy
PRA-PRCD
Progressive rod-cone degeneration (PRA-prcd) is an inherited late-onset eye disease affecting many breeds of dogs...
X-linked Progressive Retinal Atrophy
XLPRA1
X-linked progressive retinal atrophy (XLPRA1) is an inherited eye disease affecting dogs. XLPRA1 results from degeneration of photoreceptor cells in the retina...
Osteochondrodysplasia
Skeletal dwarfism
OCD
Osteochondrodysplasia (OCD) is an inherited disease that affects Miniature Poodles. The disease is characterized by stunted growth and abnormal movement...
Neonatal encephalopathy with seizures
NEWS
Neonatal encephalopathy is fatal disease in newborn puppies of Standard Poodles. The affected puppies are small and weak at birth, and often die in the first week of life...
Hair Length
L Locus, long hair, short hair
LLOK
The L locus affects the length of the hair coat of dogs due to a DNA variant in the FGF5 gene...
Dwarfism
Nanism
DWARF
Pituitary dwarfism (also called nanism) is a disease that leads to a dwarf growth of dogs and is caused by degeneration of the pituitary gland with a consequent lack of production of growth hormones...
Chondrodysplasia, chondrodystrophy and degeneration of intervertebral discs
Hansen's Type I IVDD, Intervertebral Disc Disease
CDPA/CDDY+IVDD
Chondrodysplasia (CDPA) is a genetic disease causing abnormal growth of cartilage and early changes in the structure of growth plates. The affected dogs are generally characterized by a normal sized trunk and short limbs.
Hyperuricosuria
Urolithiasis
HUU
Hyperuricosuria is characterized by an elevated levels of uric acid in the urine and can lead to the formation of bladder or kidney stones.
von Willebrand disease I
Pseudohemophilia, Vascular hemophilia
VWDI
Von Willebrand disease I (VWDI) is an inherited bleeding disorder in dogs and other mammals...
GM2 gangliosidosis
Sandhoff disease
GM2
GM2 gangliosidosis is a neurological disease usually manifesting around 9 to 12 months of age of a puppy. Symptoms include loss of vision, difficulty walking, loss of balance, head tremors and vomiting...
Dental-skeletal-retinal anomaly
DSRA
Dental skeletal retinal anomaly (DSRA) is an inherited genetic syndrome that affects dogs of the Cane Corso breed. The disease is clinically characterized by skeletal abnormalities, progressive retinal involvement leading to loss of vision, and dental imperfections...
Neuronal ceroid lipofuscinosis 1
Batten disease
NCL1
Neuronal ceroid lipofuscinosis 1 (NCL1) is a rare genetic disorder observed in one individual of Cane Corso breed...
Skeletal dysplasia 3
Disproportionate dwarfism
SD3
Skeletal dysplasia, type 3 is a new genetic disease described in Hungarian Vizslas in 2022. The disease is primarily characterized by shortening and deformation of the humerus and femur, but other long bones are also altered...
