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

Tester:

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 

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

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