Rising Phoenix

My wolfdogs are tested for the following health conditions:



Clinical:
Multidrug Sensitivity
(MDR1)
----------------------------


Blood:
 P2RY12 Defect (P2RY12)

Factor VII Deficiency (F7 Exon 5)

Factor VIII Deficiency, Hemophilia A (F8 Exon 11, Shepherd Variant 1)

Factor VIII Deficiency, Hemophilia A (F8 Exon 1, Shepherd Variant 2)

Thrombopathia (RASGRP2 Exon 8)

Thrombopathia (RASGRP2 Exon 5, American Eskimo Dog Variant)

Von Willebrand Disease Type II (VWF Exon 28)

Von Willebrand Disease Type III (VWF Exon 4)

Von Willebrand Disease Type I (VWF)

Canine Leucocyte Adhesion Deficiency Type III (FERMT3)

Canine Elliptocytosis (SPTB Exon 30)

Glanzmann's Thrombasthenia Type I (ITGA2B Exon 13)

Glanzmann's Thrombasthenia Type I (ITGA2B Exon 12)

May-Hegglin Anomaly (MYH9)

Prekallikrein Deficiency (KLKB1 Exon 8)

Pyruvate Kinase Deficiency (PKLR Exon 5)

Pyruvate Kinase Deficiency (PKLR Exon 10)

Trapped Neutrophil Syndrome (VPS13B)

Ligneous Membranitis (PLG)
----------------------------------


Hormones:
Congenital hypothyroidism
---------------------------


Immune:

Complement 3 (C3) deficiency (C3)

Severe Combined Immunodeficiency (PRKDC)

Severe Combined Immunodeficiency (RAG1)

X-linked Severe Combined Immunodeficiency (IL2RG Variant 1)

X-linked Severe Combined Immunodeficiency (IL2RG Variant 2)
--------------------------------


Eyes:

Progressive Retinal Atrophy (PRA) Rod-cone dysplasia, rcd1a (PDE6B Exon 21 Sloughi Variant)

Progressive Retinal Atrophy (PRA) Rod-cone dysplasia, rcd3 (PDE6A)

Progressive Retinal Atrophy (PRA) (CNGA1 Exon 9)

Progressive Retinal Atrophy (PRA) Progressive rod-cone degeneration (PRCD Exon 1)

Progressive Retinal Atrophy (PRA) (CNGB1)

Progressive Retinal Atrophy (PRA) (SAG)

Progressive Retinal Atrophy (PRA) Cone-rod dystrophy 1, crd1 (PDE6B)

Progressive Retinal Atrophy (PRA) Cone-rod dystrophy 2, crd2 (IQCB1)

Progressive Retinal Atrophy (PRA) Cone-rod dystrophy, crd4/cord1 (RPGRIP1)

Collie Eye Anomaly, Choroidal hypoplasia (NHEJ1)

Day blindness, Achromatopsia, Cone Degeneration (CNGB3 Exon 6)

Achromatopsia (CNGA3 Exon 7 German Shepherd Variant)

Autosomal Dominant Progressive Retinal Atrophy (RHO)

Canine Multifocal Retinopathy cmr1 (BEST1 Exon 2)

Canine Multifocal Retinopathy cmr2 (BEST1 Exon 5)

Canine Multifocal Retinopathy cmr3 (BEST1 Exon 10 Deletion)

Canine Multifocal Retinopathy cmr3 (BEST1 Exon 10 SNP)

Glaucoma Primary Open Angle Glaucoma (ADAMTS10 Exon 9)

Glaucoma Primary Open Angle Glaucoma (ADAMTS10 Exon 17)

Glaucoma Primary Open Angle Glaucoma (ADAMTS17 Exon 12)

Hereditary Cataracts, Early-Onset Cataracts, Juvenile Cataracts (HSF4 Exon 9 Boston Terrier Variant)

Primary Lens Luxation (ADAMTS17)

Congenital stationary night blindness (RPE65)
----------------------------------------------------


Kidney and Bladder:

2,8-Dihydroxyadenine (2,8-DHA) Urolithiasis (APRT)

Cystinuria Type I-A (SLC3A1)

Cystinuria Type II-A (SLC3A1)

Cystinuria Type II-B (SLC7A9)

Hyperuricosuria and Hyperuricemia or Urolithiasis (SLC2A9)

Polycystic Kidney Disease (PKD1)

Primary Hyperoxaluria (AGXT)

Protein Losing Nephropathy (NPHS1)

X-Linked Hereditary Nephropathy (COL4A5 Exon 35)

Autosomal Recessive Hereditary Nephropathy (COL4A4 Exon 30)

Autosomal Recessive Hereditary Nephropathy (COL4A4 Exon 3)
----------------------------------


Multi System:

Primary Ciliary Dyskinesia (CCDC39 Exon 3)

Congenital Keratoconjuctivitis Sicca and Ichthyosiform Dermatosis (CKCSID),

Dry Eye Curly Coat Syndrome (FAM83H Exon 5)

X-linked Ectodermal Dysplasia, Anhydrotic Ectoderal Dysplasia (EDA Intron 8)

Renal Cystadenocarcinoma and Nodular Dermatofibrosis (RCND) (FLCN Exon 7)

Glycogen Storage Disease Type II, Pompe's Disease (GAA)

Glycogen Storage Disease Type Ia, Von Gierke Disease (G6PC)

Glycogen Storage Disease Type IIIa (GSD IIIa) (AGL)

Mucopolysaccharidosis Type IIIA, Sanfilippo Syndrome Type A (SGSH Exon 6 Variant 1)

Mucopolysaccharidosis Type IIIA, Sanfilippo Syndrome Type A (SGSH Exon 6 Variant 2)

Mucopolysaccharidosis Type VII, Sly Syndrome (GUSB Exon 5)

Mucopolysaccharidosis Type VII, Sly Syndrome (GUSB Exon 3)

Glycogen storage disease Type VII, Phosphofructokinase deficiency (PFKM Exon 21)

Glycogen storage disease Type VII, Phosphofructokinase deficiency (PFKM Exon 8)

Lagotto Storage Disease (ATG4D)

Neuronal Ceroid Lipofuscinosis 1 (PPT1 Exon 8)

Neuronal Ceroid Lipofuscinosis 2 (TPP1 Exon 4)

Neuronal Ceroid Lipofuscinosis 1 (ARSG Exon 2)

Neuronal Ceroid Lipofuscinosis 1 (CLN5 Exon 4 Variant 1)

Neuronal Ceroid Lipofuscinosis 6 (CLN6 Exon 7)

Neuronal Ceroid Lipofuscinosis 8 (CLN8 Exon 2)

Neuronal Ceroid Lipofuscinosis (MFSD8)

Neuronal Ceroid Lipofuscinosis (CLN8)

Neuronal Ceroid Lipofuscinosis 10 (CTSD Exon 5)

Neuronal Ceroid Lipofuscinosis (CLN5 Exon 4 Variant 2)

Adult-Onset Neuronal Ceroid Lipofuscinosis (ATP13A2)

Gangliosidosis GM1 Gangliosidosis (GLB1 Exon 15 Shiba Inu Variant)

Gangliosidosis GM1 Gangliosidosis (GLB1 Exon 15 Alaskan Husky Variant)

Gangliosidosis GM1 Gangliosidosis (GLB1 Exon 2)

Gangliosidosis GM2 Gangliosidosis (HEXB Exon 3)

Gangliosidosis GM2 Gangliosidosis (HEXA)

Globoid Cell Leukodystrophy, Krabbe's disease (GALC Exon 5)
---------------------------------------------


Other Systems:

Autosomal Recessive Amelogenesis Imperfecta (ENAM)

Persistent Mullerian Duct Syndrome (AMHR2)
------------------------------------------


Brain and Spinal Cord:

Alaskan Husky Encephalopathy, Subacute Necrotizing Encephalomyelopathy (SLC19A3)

Alexander Disease (GFAP)

Cerebellar Abiotrophy, Neonatal Cerebellar Cortical Degeneration (SPTBN2)

Cerebellar Ataxia, Progressive Early-Onset Cerebellar Ataxia (SEL1L)

Cerebellar Hypoplasia (VLDLR)

Spinocerebellar Ataxia, Late-Onset Ataxia (CAPN1)

Spinocerebellar Ataxia with Myokymia and/or Seizures (KCNJ10)

Benign Familial Juvenile Epilepsy, Remitting Focal Epilepsy (LGI2)

Degenerative Myelopathy (SOD1 Exon 2)

Fetal-Onset Neonatal Neuroaxonal Dystrophy (MFN2)

Hypomyelination and Tremors (FNIP2)

Shaking Puppy Syndrome, X-linked Generalized Tremor Syndrome (PLP)

L-2-Hydroxyglutaricaciduria (L2HGDH)

Neonatal Encephalopathy with Seizures (NEWS) (ATF2)

Polyneuropathy (NDRG1 Exon 15)

Polyneuropathy (NDRG1 Exon 4)

Narcolepsy (HCRTR2 Intron 6)

Progressive Neuronal Abiotrophy (Canine Multiple System Degeneration) (SERAC1 Exon 15)

Progressive Neuronal Abiotrophy (Canine Multiple System Degeneration) (SERAC1 Exon 4)

Hereditary Sensory Autonomic Neuropathy (HSAN), Acral Mutilation Syndrome (GDNF-AS)
---------------------------------------------------------


Heart:

Dilated Cardiomyopathy (PDK4)

Long QT Syndrome (KCNQ1)
----------------------------------------------------------


Muscular:

Centronuclear Myopathy (PTPLA)

Exercise-Induced Collapse (DNM1)

Myotonia Congenita (CLCN1 Exon 7)

Myotonia Congenita (CLCN1 Exon 23)

Myotubular Myopathy 1, X-linked Myotubular Myopathy (MTM1)
---------------------------------------


Metabolic:

Hypocatalasia, Acatalasemia (CAT)

Pyruvate Dehydrogenase Deficiency (PDP1)

Malignant Hyperthermia (RYR1)
--------------------------------------------------


Gastro Intestinal:

Imerslund-Grasbeck Syndrome, Selective Cobalamin Malabsorption (CUBN Exon 53)

Imerslund-Grasbeck Syndrome, Selective Cobalamin Malabsorption (CUBN Exon 8)
---------------------------------------


Neuro-Muscular:

Congenital Myasthenic Syndrome (CHAT)

Congenital Myasthenic Syndrome (COLQ)

Episodic Falling Syndrome (BCAN)
-------------------------------------------------


Skin:

Dystrophic Epidermolysis Bullosa (COL7A1)

Ectodermal Dysplasia, Skin Fragility Syndrome (PKP1)

Ichthyosis, Epidermolytic Hyperkeratosis (KRT10)

Ichthyosis (PNPLA1)

Focal Non-Epidermolytic Palmoplantar Keratoderma, Pachyonychia Congenita (KRT16)

Hereditary Footpad Hyperkeratosis (FAM83G)

Hereditary Nasal Parakeratosis (SUV39H2)

Musladin-Lueke Syndrome (ADAMTSL2)
---------------------------------------


Skeletal:

Cleft Lip and/or Cleft Palate (ADAMTS20)

Hereditary Vitamin D-Resistant Rickets (VDR)

Oculoskeletal Dysplasia 1, Dwarfism-Retinal Dysplasia 1 (COL9A3)

Osteogenesis Imperfecta, Brittle Bone Disease (COL1A2)

Osteogenesis Imperfecta, Brittle Bone Disease (SERPINH1)

Osteogenesis Imperfecta, Brittle Bone Disease (COL1A1)

Osteochondrodysplasia, Skeletal Dwarfism (SLC13A1)

Skeletal Dysplasia 2 (COL11A2)