Namn: SE*LovelyPaw's Minna
Född: 2020-03-26
Färg: a 09
Far: IC S*Lockhart's IgelkottsRos of Huggis
Mor: GIC S*Oblivion's Rainbow Dash

HCM: NORMAL 26/3-21
Patella: UA 26/3-21

Tester:

50 CLEAR tests result via MY CATDNA

Acute Intermittent Porphyria (Variant 1)

Acute intermittent porphyria (AIP) is a disorder caused by decreased cellular enzymatic activity leading to an accumulation of byproducts, called porphyrins, in the tissues. The disease is characterized by the brownish coloration of the teeth and brownish urine of affected cats.

Acute Intermittent Porphyria (Variant 2)

Acute intermittent porphyria (AIP) is a disorder caused by decreased cellular enzymatic activity leading to an accumulation of byproducts, called porphyrins, in the tissues. The disease is characterized by the brownish coloration of the teeth and brownish urine of affected cats.

Acute Intermittent Porphyria (Variant 3)

Acute intermittent porphyria (AIP) is a disorder caused by decreased cellular enzymatic activity leading to an accumulation of byproducts, called porphyrins, in the tissues. The disease is characterized by the brownish coloration of the teeth and brownish urine of affected cats.

Acute Intermittent Porphyria (Variant 4)

Acute intermittent porphyria (AIP) is a disorder caused by decreased cellular enzymatic activity leading to an accumulation of byproducts, called porphyrins, in the tissues. The disease is characterized by the brownish coloration of the teeth and brownish urine of affected cats.

Acute Intermittent Porphyria (Variant 5)

Acute intermittent porphyria (AIP) is a disorder caused by decreased cellular enzymatic activity leading to an accumulation of byproducts, called porphyrins, in the tissues. The disease is characterized by the brownish coloration of the teeth and brownish urine of affected cats.

Autoimmune Lymphoproliferative Syndrome

Autoimmune Lymphoproliferative Syndrome is an immunologic disorder characterized by severely enlarged lymph nodes.

Burmese Head Defect (Discovered in the Burmese)

Burmese Head Defect is a disorder where cats with two copies of the mutation will be born with severe facial defects requiring humane euthanasia shortly after birth.

Chediak-Higashi Syndrome (Discovered in the Persian)

Chediak-Higashi Syndrome (CHS) is a metabolic disoder that causes partial albinism, sensitivity to light, cataracts at an early age, and prolonged bleeding.

Congenital Adrenal Hyperplasia

Congenital adrenal hyperplasia is an endocrine disorder that causes excessive drinking and urination, abnormalities of the genitallia, and aggression.

Congenital Erythropoietic Porphyria

Congenital Erythropoietic Porphyria (CEP) is a disorder caused by decreased cellular enzymatic activity leading to an accumulation of byproducts, called porphyrins, in the tissues. The disease is characterized by the brownish coloration of the teeth and brownish urine of affected cats.

Congenital Myasthenic Syndrome (Discovered in the Devon Rex and Sphynx)

Congenital Myasthenic Syndrome (CMS) is a neuromuscular disorder characterized by muscle weakness and fatigue.

Cystinuria Type 1A

Cystinuria is a metabolic disorder which predisposes the affected cat to form cystine crystals and stones within the urinary tract, which can then cause irritation and blockage.

Cystinuria Type B (Variant 1)

Cystinuria is a metabolic disorder which predisposes the affected cat to form cystine crystals and stones within the urinary tract, which can then cause irritation and blockage.

Cystinuria Type B (Variant 2)

Cystinuria is a metabolic disorder which predisposes the affected cat to form cystine crystals and stones within the urinary tract, which can then cause irritation and blockage.

Cystinuria Type B (Variant 3)

Cystinuria is a metabolic disorder which predisposes the affected cat to form cystine crystals and stones within the urinary tract, which can then cause irritation and blockage.

Dihydropyrimidinase Deficiency

Dihydropyrimidinase deficiency is a metabolic disorder that causes tiredness, weakness, vomiting, and high levels of ammonia in the blood.

Earfold and Osteochondrodysplasia (Discovered in the Scottish Fold)

Earfold and osteochondrodysplasia (discovered in the Scottish Fold) is the condition behind the breed defining folded ears; however, it also associated with skeletal malformations and arthritis.

Factor XII Deficiency (Variant 1)

Factor XII deficiency is a common blood factor deficiency in cats which does not result in an abnormal tendency to bleed but may have an effect on blood clot stability.

Factor XII Deficiency (Variant 2)

Factor XII deficiency is a common blood factor deficiency in cats which does not result in an abnormal tendency to bleed but may have an effect on blood clot stability.

Familial Episodic Hypokalemic Polymyopathy (Discovered in the Burmese)

Familial Episodic Hypokalaemic Polymyopathy is a disorder that causes skeletal muscle weakness and pain that is episodic in nature.

GM1 Gangliosidosis

GM1 Gangliosidosis is a disorder characterized by progressive nervous system degeneration with signs including incoordination of movements and tremors.

GM2 Gangliosidosis

GM2 Gangliosidosis is a disorder characterized by progressive nervous system degeneration with signs including incoordination of movements and tremors.

GM2 Gangliosidosis Type II (Discovered in Domestic Shorthair cats)

GM2 Gangliosidosis Type II is a disorder characterized by progressive nervous system degeneration with signs including incoordination of movements and tremors.

GM2 Gangliosidosis Type II (Discovered in Japanese domestic cats)

GM2 Gangliosidosis Type II is a disorder characterized by progressive nervous system degeneration with signs including incoordination of movements and tremors.

GM2 Gangliosidosis Type II (Discovered in the Burmese)

GM2 Gangliosidosis Type II is a disorder characterized by progressive nervous system degeneration with signs including incoordination of movements and tremors.

Glutaric Aciduria Type II

Glutaric Aciduria Type II is a rare metabolic disorder that causes organic acids to accumulate in the blood and urine.

Glycogen Storage Disease (Discovered in the Norwegian Forest Cat)

Glycogen Storage Disease Type IV is a disorder that affects the metabolism of glycogen resulting in low blood sugar levels and progressive neuromuscular disease.

Hemophilia B (Variant 1)

Hemophilia B, also known as Factor IX Deficiency, is a blood clotting disorder more commonly seen in males, which can result in tiredness, decreased appetite, fever, lameness, and prolonged bleeding times after injury, trauma or surgery.

Hemophilia B (Variant 2)

Hemophilia B, also known as Factor IX Deficiency, is a blood clotting disorder more commonly seen in males, which can result in tiredness, decreased appetite, fever, lameness, and prolonged bleeding times after injury, trauma or surgery.

Hyperoxaluria Type II

Hyperoxaluria is a kidney disorder leading to profound weakness and acute kidney disease at a young age.

Hypertrophic Cardiomyopathy (Discovered in the Maine Coon)

Hypertrophic cardiomyopathy is a disorder where the heart muscle wall increases in thickness, eventually leading to heart failure.

Hypertrophic Cardiomyopathy (Discovered in the Ragdoll)

Hypertrophic cardiomyopathy is a disorder where the heart muscle wall increases in thickness, eventually leading to heart failure.

Hypotrichosis (Discovered in the Birman)

Hypotrichosis is a disorder of the immune system causing kittens to be born hairless and to develop serious infections.

Lipoprotein Lipase Deficiency

Lipoprotein Lipase Deficiency is a metabolic disorder that causes reduced body mass and growth rates in kittens, lipemia (excessive fatty substances in the blood), and increased stillbirth rates.

MDR1 Medication Sensitivity

Medication Sensitivity (or Multidrug Resistance 1) is a disorder resulting from a defective drug pumping protein that plays an important role in limiting drug absorption and distribution (particularly to the brain). Cats with the ABCB1 mutation may have severe adverse reactions to some commonly used medications.

Mucopolysaccharidosis Type I

Mucopolysaccharidosis Type I is a disorder causing failure to thrive, facial and other skeletal abnormalities, tremors, and corneal clouding.

Mucopolysaccharidosis Type VI (Variant 1)

Mucopolysaccharidosis VI is a lysosomal storage disease resulting in a degenerative joint disease. This mutation (the G1558A variant) may cause for a mild form of the disease, but only if one copy of the severe disease variant (the T1427C variant) is also present.

Mucopolysaccharidosis Type VI (Variant 2)

Mucopolysaccharidosis Type VI is a disorder causing dwarfism, degenerative joint disease, and corneal clouding.

Mucopolysaccharidosis Type VII (Variant 1)

Mucopolysaccharidosis Type VII is a disorder causing weakness, growth retardation, facial and other skeletal abnormalities, and corneal clouding.

Mucopolysaccharidosis Type VII (Variant 2)

Mucopolysaccharidosis Type VII is a disorder causing weakness, growth retardation, facial and other skeletal abnormalities, and corneal clouding.

Myotonia Congenita

Myotonia Congenita is a neuromuscular disorder that affects cats from birth, causing stiff movement and delayed relaxation of muscles after exercise.

Polycystic Kidney Disease (PKD)

Polycystic kidney disease is the most common inherited disease in cats. The disease causes the formation of fluid-filled cysts in the kidneys that can lead to kidney failure.

Progressive Retinal Atrophy (Discovered in the Abyssinian)

Progressive Retinal Atrophy (PRA) is a disorder that causes the degeneration of the light sensing retina at the back of the eye, resulting in vision loss.

Progressive Retinal Atrophy (Discovered in the Bengal)

Bengal Progressive Retinal Atrophy (PRA) is an eye disorder that causes the degeneration of the light sensing retina at the back of the eye, resulting in vision loss.

Progressive Retinal Atrophy (Discovered in the Persian)

Persian Progressive Retinal Atrophy (PRA) is an eye disorder that causes the degeneration of the light sensing retina at the back of the eye, resulting in vision loss.

Pyruvate Kinase Deficiency

Pyruvate Kinase (PK) Deficiency is a disorder that causes anemia due to the breakdown of red blood cells.

Sphingomyelinosis (Variant 1)

Sphingomyelinosis (Mutation 1) is a neurological disorder that causes progressively severe neurologic signs, enlargement of the spleen and liver, and changes in the lungs.

Sphingomyelinosis (Variant 2)

Sphingomyelinosis (Mutation 2) is a neurological disorder that causes progressively severe neurologic signs and reduced menace response.

Spinal Muscular Atrophy (Discovered in the Maine Coon)

Spinal muscular atrophy is a muscular disorder that causes muscle wasting and progressive weakness. Please note that this test detects presence or absence of the disease mutation and cannot distinguish cats that have one copy of the disease mutation from cats with two copies of the disease mutation.

Vitamin D-Dependent Rickets

Vitamin D-Dependent Rickets (VDDR) is a metabolic disorder resulting in low blood.

Namn: SE*LovelyPaw's Lissie
Född: 2020-02-28
Färg: f 21 32
Far: IC SE*Lovling Nest I Zico
Mor: CH SE*LovelyPaw's Inca 


Patella: UA
HCM: NORMAL 15/3-21

Tester:

Namn: CH SE*LovelyPaw's Inca
Född: 2018-07-14
Färg: a 32
Far: IC S*Lockhart's PlommonRos of Sotis
Mor: GIC S*Oblivion's Rainbow Dash

Tester:
PKD: Normal
CMS: Normal
HCM: Normal
Patella: Normal
HD:
Höger sida: Normal
Vänster sida: Normal

GIC SE*Oblivion's Rainbow Dash
Titel: Grand Int. Champion
Född 2016-03-15
Färg blå skölpadspotted
Far Devenly's Ray of Light
Mor Oblivion's Emmylou

Tester:
HCM: Normal

Namn: SE*LovelyPaw's Jasmine

Född: 2019-01-29
Färg: f 24
Far: S*Zwelaboz Mandel
Mor: GIC SE*Oblivion's Rainbow Dash

HCM: UA 2/9-20
Patella: UA 30/3-21

Tester:
Eder (proglottider) av bandmask EJ påvisade
Parasitägg eller coccidier EJ påvisade
Ingen förekomst av cystor av Giardia eller oocystor av Cryptosporidium Immunofluorescens (IF)
Tritrichomonas foetus, nukleinsyra EJ påvisad

Blodgrupp: B

Hälsotester:
Muscular Disorders
Congenital Myasthenic Syndrome
(CMS) G/G CLEAR

Ocular Disorders Retinal Dystrophy (rdAc ) T/T CLEAR
Blood Disorders Erythrocyte Pyruvate Kinase
(PK) Deficiency CLEAR
Blood Disorders Factor XII Deficiency CLEAR
Blood Disorders Hemophilia B, mutation F9: c.1014C>T CLEAR
Blood Disorders Hemophilia B, mutation F9: c.247G>A CLEAR
Blood Disorders Hemophilia B, mutation F9: c.247G>A CLEAR
Cardiac Disorders Hypertrophic Cardiomyopathy, MYBPC3 mutation: A31P found in Maine Coon
CLEAR

Cardiac Disorders Hypertrophic Cardiomyopathy, MYBPC3 mutation: c.2460C>T found in Ragdoll
CLEAR

Endocrine Disorders Congenital Adrenal Hyperplasia CLEAR

Immunologic Disorders Autoimmune Lymphoproliferative Syndrome CLEAR
Immunologic Disorders Congenital Hypotrichosis with Short Life Expectancy CLEAR

Metabolic Disorders Acute Intermittent Porphyria CLEAR
Metabolic Disorders Acute Intermittent Porphyria; HMBS mutation: c.107_110delACAG CLEAR
Metabolic Disorders Acute Intermittent Porphyria; HMBS mutation: c.826-1G>A CLEAR
Metabolic Disorders Acute Intermittent Porphyria; HMBS mutation: c.844delGAG CLEAR
Metabolic Disorders Chylomicronemia, Lipoprotein Lipase Deficiency CLEAR
Metabolic Disorders Congenital Erythropoietic Porphyria, mutation UROS: c.331G>A CLEAR
Metabolic Disorders Cystinuria; SCL3A1 mutation CLEAR
Metabolic Disorders Cystinuria; SCL7A9 mutation: c.1175C>T CLEAR
Metabolic Disorders Cystinuria; SCL7A9 mutation: c.706G>A CLEAR
Metabolic Disorders Cystinuria; SCL7A9 mutation: c.881A>T CLEAR
Metabolic Disorders Dihydropyrimidinuria CLEAR
Metabolic Disorders Mucopolysaccharidosis Type I CLEAR
Metabolic Disorders Mucopolysaccharidosis Type VI (MPS VI), Typical Form CLEAR
Metabolic Disorders Mucopolysaccharidosis Type VII, mutation GUSB: c.1074G>A CLEAR
Metabolic Disorders Mucopolysaccharidosis VII; GUSB mutation C1424T CLEAR
Metabolic Disorders Vitamin D-Dependent Rickets (VDDR-1A); CYP27B mutation: c.G637T CLEAR

Muscuelar Disorders Myotonia Congenita CLEAR
Muscular Disorders Periodic Hypokalemic Polymyopathy, Burmese Hypokalemia, or Familial Episodic Hypokalaemic Polymyopathy CLEAR
Muscular Disorders Spinal Muscular Atrophy (SMA)/Spinal Muscular Dystrophy CLEAR

Neurologic Disorders Feline GM1 Gangliosidosis CLEAR
Neurologic Disorders GM2 Gangliosidosis, Domestic Shorthair mutation HEXB: c.1467_1491inv CLEAR
Neurologic Disorders GM2 Gangliosidosis, Japanese Domestic mutation HEXB: c.667C>T CLEAR
Neurologic Disorders GM2 Gangliosidosis; Domestic Shorthair GM2A Mutation CLEAR
Neurologic Disorders Niemann-Pick C2, NPC Disease, Sphingomyelinosis NPC2 Mutation CLEAR
Neurologic Disorders Niemann–Pick C1, NPC Disease, Sphingomyelinosis NPC1 Mutation CLEAR

Neuromuscular Disorders Glycogen Storage Disease Type IV CLEAR

Ocular Disorders Bengal Progressive Atrophy CLEAR

Renal Disorders Hyperoxaluria CLEAR
Renal Disorders Polycystic Kidney Disease CLEAR

Skeletal Disorders Burmese Head Defect CLEAR
Skeletal Disorders Osteochondrodysplasia and Folded Ears; TRPV4 mutation p.V342F CLEAR

BOR HOS FODERVÄRD