Immune Clearances:
Complement 3 (C3) Deficiency - CLEAR/NORMAL
Severe Combined Immunodeficiency - PRKDC - CLEAR/NORMAL
Severe Combined Immunodeficiency - RAG1 - CLEAR/NORMAL
X-Linked Severe Combined Immunodeficiency - Variant 1 - CLEAR/NORMAL
X-Linked Severe Combined Immunodeficiency - Variant 2 - CLEAR/NORMAL
Hormone Clearances:
Congenital Hypothyroidism - CLEAR/NORMA
L
Kidney & Bladder Clearances:
2, 8-Dihydroxyadenine (2,80DHA) Urolithiasis - CLEAR/NORMAL
Cystinuria Type I-A - SLC3A1 - CLEAR/NORMAL
Cystinuria Type I-A - SLC7A9 - CLEAR/NORMAL
Cystinuria Type II-A - CLEAR/NORMAL
Hyperuricosuria & Hyperuricemia or Urolithiasis - CLEAR/NORMAL
Polycystic Kidney Disease - CLEAR/NORMAL
Primary Hyperoxaluria - CLEAR/NORMAL
Protein Losing Nephropathy - CLEAR/NORMAL
X-Linked Hereditary Nephropathy (Variant 2) - CLEAR/NORMAL
Autosomal Recessive Hereditary Nephropathy (Familial Nephropathy) - CLEAR/NORMAL
Other Health Clearances:
Autosomal Recessive Amelogenesis Imperfecta - CLEAR/NORMAL
Persistent Mullerian Duct Syndrome - CLEAR/NORMAL
Deafness & Vestibular Syndrome - CLEAR/NORMAL
Autoinflammatory Disease - CLEAR/NORMAL
BRAIN & SPINAL CORD CLEARANCES:
Alexander Disease - CLEAR/NORMAL
Encephalopathy, Subacute Necrotizing Encephalomyelopathy - CLEAR/NORMAL
Cerebellar Abiotrophy, Neonatal Cerebellar Cortical Degeneration - CLEAR/NORMAL
Cerebellar Ataxia, Progressive Early-Onset Cerebellar Ataxia - CLEAR/NORMAL
Cerebellar Hypoplasia - CLEAR/NORMAL
Spinocerebellar Ataxia, Late-Onset Ataxia - CLEAR/NORMAL
Spinocerebellar Ataxia with Myokymia and/or Seizures - CLEAR/NORMAL
Benign Familial Juvenile Epilepsy, Remitting Focal Epilepsy - CLEAR/NORMAL
Degenerative Myelopathy - CLEAR/NORMAL
Fetal-Onset Neonatal Neuroaxonal Dystrophy - CLEAR/NORMAL
Hypomyelination & Tremors - CLEAR/NORMAL
Shaking Puppy Syndrome, X-Linked Generalized Tremor Syndrome - CLEAR/NORMAL
L-2-Hydroxyglutaric Aciduria - CLEAR/NORMAL
Neonatal Encephalopathy with Seizures (NEWS) - CLEAR/NORMAL
Polyneuropathy, NDRG1 Exon 15 - CLEAR/NORMAL
Polyneuropathy, NDRG1 Exon 4 - CLEAR/NORMAL
Narcolepsy - CLEAR/NORMAL
Progressive Neuronal Abiotrophy (canine Multiple System Degeneration) Exon 4 - CLEAR/NORMAL
Progressive Neuronal Abiotrophy (canine Multiple System Degeneration) Exon 15 - CLEAR/NORMAL
Juvenile Laryngeal Paralysis & Polyneuropathy, Polyneuropathy with Ocular Abnormalities & Neuronal Vacuolation (POANV) - CLEAR/NORMAL
Hereditary Sensory Autonomic Neuropathy (HSAN), Acral Mutilation Syndrome - CLEAR/NORMAL
Juvenile Onset Polyneuropathy, Leonberger Polyneuropathy 1 - CLEAR/NORMAL
Spongy Degeneration with Cerebellar Ataxia 1, SeSAME/EAST - CLEAR/NORMAL
Spongy Degeneration with Cerebellar Ataxia 2, SeSAME/EAST - CLEAR/NORMAL
HEART CLEARANCES:
Dilated Cardiomyopathy - CLEAR/NORMAL
Long QT Syndrome - CLEAR/NORMAL
MUSCULAR CLEARANCES: Muscular Dystrophy - CLEAR/NORMAL
Centronuclear Myopathy - CLEAR/NORMAL
Exercise-Induced Collapse - CLEAR/NORMAL
Inherited Myopathy - CLEAR/NORMAL
Myostatin Deficiency - CLEAR/NORMAL
Myotonia Congenita Exon 7 - CLEAR/NORMAL
Myotonia Congenita Exon 23 - CLEAR/NORMAL
Myotubular Myopathy 1, X-linked Myotubular Myopathy - CLEAR/NORMAL
METABOLIC CLEARANCES:
Hypocatalasia, Acatalasemia - CLEAR/NORMAL
Pyruvate Dehydrogenase Deficiency - CLEAR/NORMAL
Malignant Hyperthermia - CLEAR/NORMAL
GASTROINTESTINAL CLEARANCES:
Imerslund-Grasbeck Syndrome, Selective Cobalamin Malabsorption Exon 8 - CLEAR/NORMAL
Imerslund-Grasbeck Syndrome, Selective Cobalamin Malabsorption Exon 53 - CLEAR/NORMAL
NEUROMUSCULAR CLEARANCES: Congenital Myasthenic Syndrome CHAT - CLEAR/NORMAL
Congenital Myasthenic Syndrome COLQ - CLEAR/NORMAL
Episodic Falling Syndrome - CLEAR/NORMAL
SKIN & CONNECTIVE TISSUES CLEARANCES:
Dystrophic Epidermolysis BUllosa - CLEAR/NORMAL
Ectodermal Dysplasia, SKin Fragility SYndrome - CLEAR/NORMAL
Ichthyosis, Epidermolytic Hyperkeratosis - CLEAR/NORMAL
Ichthyosis PNPLA1 - CLEAR/NORMAL
Ichthyosis SLC27A4 - CLEAR/NORMAL
Ichthyosis NIPAL4 - CLEAR/NORMAL
Focal Non-Epidermolytic Palmoplantar Keratoderma, Pachyonychia Congenita - CLEAR/NORMAL
Hereditary Footpad Hyperkeratosis - CLEAR/NORMAL
Hereditary Nasal Parakeratosis HNPK - CLEAR/NORMAL
Musladin-Lueke Syndrome - CLEAR/NORMAL
SKELETAL CLEARANCES:
Cleft Lip and/or Cleft Palate - CLEAR/NORMAL
Hereditary Vitamin D-Resistant Rickets - CLEAR/NORMAL
Oculoskeletal Dysplasia 1, Dwarfism-Retinal Dysplasia - CLEAR/NORMAL
Osteogenesis Imperfecta, Brittle Bone Disease (COL1A1) - CLEAR/NORMAL
Osteogenesis Imperfecta, Brittle Bone Disease (COL1A2) - CLEAR/NORMAL
Osteogenesis Imperfecta, Brittle Bone Disease (SERPINH1) - CLEAR/NORMAL
Osteochondrodysplasia, Skeletal Dwarfism - CLEAR/NORMAL
Skeletal Dysplasia 2 - CLEAR/NORMAL
Craniomandibular Osteopathy (CMO) - CLEAR/NORMAL
COAT COLOR CLEARANCES:
E Locus (MC1R) - No dark hairs anywhere
D Locus (MLPH) Does not carry Dilute - CLEAR/NORMAL
B Locus (TYRP1) Produces Black pigment in skin, noses, eye rims and footpads
We are happy to share photos of Powder's dam & sire, with permission