Reminder: Login to access new features and members-only content!

Register to be a member of our community. Its easy!

Register a new account

Already a member?

Log In here!

Donate

Did you find our content interesting or helpful? Help support the IPFD enhance health, well-being and welfare for dogs everywhere.

Jump to content
WATCH NOW: Full video from recent webinar - "Breeding Healthy, Quality Dogs: The Veterinarian, Breeder, and Public Roles" w/ Jerold S Bell, DVM ×

VetGen LLC

Non-Participant

General Information

Name
VetGen LLC
Data Up to Date
2019
GTP Code
VG
URL
http://www.vetgen.com
Email
vetgen@vetgen.com
Telephone
1-800-483-8436 (US/CA), or 734-669-8440
Address
3728 Plaza Drive, Suite 1
City
Ann Arbor
State
Michigan
Zip Code/ Postal Code
48108
Country
United States
Participant Since:
2018

People

Qualified Laboratory Technicians
Data not available

Quality Indicators - GTP

Non-Participant
Out Sourced Lab(s) in HGTD
Data not available
Laboratory SOPs
Data not available
GTP Service Description
Data not available
Outsourced Lab(s) Accredited
Data not available

Quality Indicators - Procedures/ Services

Test Faults Protocol
Data not available

Research

Ethics Committee/Board
Data not available

Phenes

Achromatopsia 2
Acral Mutilation Syndrome
Alpha Fucosidosis
Asymptomatic Macrothrombocytopenia
Ataxia, cerebellar, ATP1B2-related
Ataxia, Cerebellar, Juvenile to Adolescent, RAB24-related
Ataxia, Cerebellar, Neonatal, GRM1-related
Ataxia, Spinocerebellar, CAPN1-related
Canine Cyclic Neutropenia (Grey Collie Syndrome)
Canine Leukocyte Adhesion Deficiency (CLAD)
Canine Multifocal Retinopathy 1 (cmr1)
Canine Multifocal Retinopathy 2 (cmr2)
Canine Multiple System Degeneration (CMSD)
Centronuclear Myopathy
Cerebellar Hypoplasia, VLDLR-associated
Chondrodysplasia, Disproportionate Short-limbed
Chondrodystrophy (CDDY and IVDD)
Coat Colour, Albinism, Oculocutaneous Type IV
Congenital Hypothyroidism
Congenital Myasthenic Syndrome - CHRNE related
Congenital Myasthenic Syndrome - COLQ related
Copper Toxicosis, ATP7B Type
Craniomandibular Osteopathy
Curly Coat Dry Eye (CKCSID)
Cystinuria Type I-A
Cystinuria Type II-B
Degenerative Myelopathy
Dental Hypomineralization
Dermatomyositis
Dwarfism, Pituitary
Dystrophic Epidermolysis Bullosa
Ectodermal Dysplasia
Ectodermal Dysplasia XHED, XLED
Episodic Falling
Exercise-Induced Collapse / EIC
Factor IX Deficiency
Factor VII Deficiency
Factor VIII Deficiency
Factor XI Deficiency
Gastric Dilatation-volvulus (GDV) - Bloat
Glanzmann Thrombasthenia Type I
Globoid Cell Leukodystrophy
Glycogen Storage Disease VII (GSD VII)
GM1 Gangliosidosis
GM2 Gangliosidosis
GM2 Gangliosidosis Type I (B Variant)
Hereditary Footpad Hyperkeratosis
Hyperuricosuria and Hyperuricemia (HUU)
Hypocatalasia (Acatalasemia)
Hypomyelination
Ichthyosis, NIPAL4-related
Imerslund-Grasbeck Syndrome (I-GS), AMN-related
Imerslund-Grasbeck Syndrome (I-GS), CUBN related
Juvenile Dilated Cardiomyopathy
Juvenile Laryngeal Paralysis and Polyneuropathy (JLPP)
L-2-Hydroxyglutaric Aciduria (L-2-HGA)
Leukoencephalomyelopathy (LEMP)
Macular Corneal Dystrophy
Malinois Episodic Aggression
May-Hegglin Anomaly
Mucopolysaccharidosis Type I
Mucopolysaccharidosis Type IIIA
Mucopolysaccharidosis Type VI
Mucopolysaccharidosis Type VII
Multidrug Resistance 1 (MDR1)
Muscular Dystrophy (Duchenne-type, DMD) GRMD
Musladin-Lueke Syndrome
Myotubular Myopathy 1 (XLMTM)
Narcolepsy
Nasal Parakeratosis
Necrotising Encephalopathy, Subacute, of Leigh
Neonatal Encephalopathy with Seizures
Nephritis, X-linked
Neuroaxonal Dystrophy (Fetal-onset, FNAD)
Neuroaxonal Dystrophy, Juvenile
Neuroaxonal Dystrophy (NAD)
Neuronal Ceroid Lipofuscinosis 10 (NCL10)
Neuronal Ceroid Lipofuscinosis 12 (NCL12)
Neuronal Ceroid Lipofuscinosis 1 (NCL1)
Neuronal Ceroid Lipofuscinosis 2 (NCL2)
Neuronal Ceroid Lipofuscinosis 4a (NCL4a)
Neuronal Ceroid Lipofuscinosis 5 (NCL5)
Neuronal Ceroid Lipofuscinosis 6 (NCL6)
Neuronal Ceroid Lipofuscinosis 7 (NCL7)
Neuronal Ceroid Lipofuscinosis 8 (NCL8)
Neuropathy, Sensory
Neuropathy, Sensory Ataxic
Osteochondrodysplasia
Osteogenesis Imperfecta
Osteogenesis imperfecta, type III, COL1A1-related
Persistent Mullerian Duct Syndrome
Polycystic Kidney Disease
Polyneuropathy - NDRG1 Type (AMPN)
Postoperative Hemorrhage
Prekallikrein Deficiency
Primary Ciliary Dyskinesia
Primary Hereditary Cataract (PHC)
Primary Hyperoxaluria
Primary Lens Luxation (PLL)
Primary Open Angle Glaucoma (POAG) ADAMTS10
Primary Open Angle Glaucoma (POAG) ADAMTS17
Progressive Retinal Atrophy Autosomal Dominant (ADPRA)
Progressive Retinal Atrophy, CNGA1
Progressive Retinal Atrophy - CNGB1
Progressive Retinal Atrophy crd4 (PRA crd4) / cord1
Progressive Retinal Atrophy, GR PRA2
Progressive Retinal Atrophy, PRA1
Progressive Retinal Atrophy (PRA-prcd)
Progressive Retinal Atrophy rcd1 (PRA-rcd1)
Progressive Retinal Atrophy rcd3 (PRA-rcd3)
Progressive Retinal Atrophy rcd4 (PRA rcd4)
Progressive Retinal Atrophy, Type 3
Pyruvate Dehydrogenase Deficiency
Pyruvate Kinase Deficiency
Renal Cystadenocarcinoma and Nodular Dermatofibrosis
Severe Combined Immunodeficiency Disease (SCID)
Skeletal Dysplasia 2 (SD2)
Spinal Dysraphism
Spongy Degeneration with Cerebella Ataxia Subtype 1, KCNJ10-related
Tail length, Short
Thrombopathia (CalDAG-GEFI)
Tremor, X-linked
Von Willebrand Disease I
Von Willebrand Disease II
Von Willebrand Disease III
X-linked Severe Combined Immunodeficiency Disease (XSCID)
×
×
  • Create New...

Important Information

By using this site, you agree to our Terms of Use.

  I accept