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INNO

Out Sourced Testing Subsidiary Company

General Information

Name
INNO
Alternative Name
Part of Dr. van Haeringen Laboratorium B.V. (VHL)
Data Up to Date
20-Jan
GTP Code
INNO
URL
http://www.inno.pt
Email
geral@inno.pt
Telephone
+351 253 615 020
Address
Rua Cândido de Sousa 15
City
Braga
Zip Code/ Postal Code
47110-503
Country
Portugal
Participant Since:
2019
Subsidiary Company

People

Qualified Laboratory Technicians
Data not available

Quality Indicators - GTP

Out Sourced Testing
Out Sourced Lab(s) in HGTD
Yes
Laboratory SOPs
Data not available
GTP Service Description
No in house testing
Outsourced Lab(s) Accredited
Yes
Out Sourced Labs More Info
Dr. van Haeringen Laboratorium B.V

Quality Indicators - Procedures/ Services

Test Faults Protocol
Data not available

Research

Ethics Committee/Board
Data not available

Phenes

Achromatopsia 2
Achromatopsia (cone degeneration, hemeralopia), GSPT
Acrodermatitis, Lethal (LAD)
Alexander Disease
Alpha Fucosidosis
Amelogenesis Imperfecta
Asymptomatic Macrothrombocytopenia
Ataxia, cerebellar, ATP1B2-related
Ataxia, Cerebellar, Neonatal, GRM1-related
Ataxia, Spinocerebellar, CAPN1-related
Bernard-Soulier Syndrome (BSS)
Breed Diversity
Breed/Type/Variety Identification
C3 Deficiency
Canine Cyclic Neutropenia (Grey Collie Syndrome)
CanineHD Whole-Genome Genotyping
Canine Leukocyte Adhesion Deficiency (CLAD)
Canine Multifocal Retinopathy 1 (cmr1)
Canine Multifocal Retinopathy 2 (cmr2)
Canine Multifocal Retinopathy 3 (cmr3)
Centronuclear Myopathy
Cerebellar Ataxia
Cerebellar Ataxia Norwegian Buhund
Chondrodysplasia (CDPA)
Chondrodysplasia, Disproportionate Short-limbed
Coat Colour, Agouti
Coat Colour, Albinism, Oculocutaneous Type IV
Coat Colour Brown
Coat Colour Dilution, dilution, MLPH-related
Coat Colour, Dominant Black
Coat Colour Em-locus
Coat Colour, Extension
Coat Colour H-locus (Harlequin)
Coat Colour Merle
Coat Colour Panda White Spotting
Coat Colour Saddle Tan vs Black-and-Tan
Collie Eye Anomaly (CEA/CH)
Congenital Hypothyroidism
Congenital Myasthenic Syndrome - CHRNE related
Congenital Stationary Night Blindness (CSNB)
Copper Toxicosis, ATP7B Type
Copper Toxicosis, COMMD1 Type
Craniomandibular Osteopathy
Curly Coat
Curly Coat Dry Eye (CKCSID)
Cystinuria Type I-A
Cystinuria Type II-A
Cystinuria Type II-B
Degenerative Myelopathy
Dental Hypomineralization
Dilated Cardiomyopathy, (DCM) DCM1 variant; Doberman Pinscher
Dilated Cardiomyopathy, (DCM); Schnauzer
DNA Banking
DNA Profile Dog
Dwarfism, Pituitary
Dystrophic Epidermolysis Bullosa
Ectodermal Dysplasia XHED, XLED
Epidermolytic Hyperkeratosis
Episodic Falling
Exercise-Induced Collapse / EIC
Factor VII Deficiency
Factor VIII Deficiency
Factor XI Deficiency
Familial Fatal Acute Respiratory Distress Syndrome (ARDS)
Furnishings (moustache and eyebrows)
Gallbladder Mucoceles
Glanzmann Thrombasthenia Type I
Globoid Cell Leukodystrophy
Glycogen Storage Disease Type Ia (GSD Ia)
Glycogen Storage Disease Type II (GSD II)
GM1 Gangliosidosis
GM2 Gangliosidosis
Goniodysgenesis and Glaucoma Susceptibility
Hair, Long
Hyperuricosuria and Hyperuricemia (HUU)
Hypocatalasia (Acatalasemia)
Hypomyelination
Ichthyosis, PNPLA1-related
Imerslund-Grasbeck Syndrome (I-GS), AMN-related
Improper Coat/Furnishings
L-2-Hydroxyglutaric Aciduria (L-2-HGA)
Lagotto Storage Disease
Leukocyte Adhesion Deficiency III (LAD3)
Malignant Hyperthermia
Maternity Verification Dog
Mucopolysaccharidosis Type IIIA
Mucopolysaccharidosis Type VII
Multidrug Resistance 1 (MDR1)
Muscular Dystrophy
Muscular Dystrophy (Duchenne-type, DMD) GRMD
Muscular Hypertrophy
Musladin-Lueke Syndrome
Myoclonus Epilepsy of Lafora
Myotonia Congenita
Myotubular Myopathy 1 (XLMTM)
Narcolepsy
Nasal Parakeratosis
Neonatal Encephalopathy with Seizures
Neuroaxonal Dystrophy (Fetal-onset, FNAD)
Neuroaxonal Dystrophy (NAD)
Neuronal Ceroid Lipofuscinosis 10 (NCL10)
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 Ataxic
Osteochondrodysplasia
Osteogenesis Imperfecta
Osteogenesis imperfecta, type III, COL1A1-related
Parentage Verification Dog
Paternity Verification Dog
Persistent Mullerian Duct Syndrome
Piebald, Extreme White Spotting
Polycystic Kidney Disease
Polyneuropathy - NDRG1 Type (AMPN)
Postoperative Hemorrhage
Prekallikrein Deficiency
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
Progressive Retinal Atrophy Autosomal Dominant (ADPRA)
Progressive Retinal Atrophy - CNGB1
Progressive Retinal Atrophy crd
Progressive Retinal Atrophy crd1 (PRA crd1)
Progressive Retinal Atrophy crd2 (PRA crd2)
Progressive Retinal Atrophy crd4 (PRA crd4) / cord1
Progressive Retinal Atrophy, GR PRA2
Progressive Retinal Atrophy, PRA1
Progressive Retinal Atrophy (PRA-prcd)
Progressive Retinal Atrophy rcd1a (PRA rcd1a)
Progressive Retinal Atrophy rcd1 (PRA-rcd1)
Progressive Retinal Atrophy rcd2 (PRA-rcd2)
Progressive Retinal Atrophy rcd3 (PRA-rcd3)
Progressive Retinal Atrophy rcd4 (PRA rcd4)
Progressive Retinal Atrophy; Swedish Vallhund
Progressive Retinal Atrophy, Type A
Progressive Retinal Atrophy, Type B
Progressive Retinal Atrophy X-linked Type 1 (XLPRA)
Protein Losing Nephropathy
Pyruvate Dehydrogenase Deficiency
Pyruvate Kinase Deficiency
Scott Syndrome
Severe Combined Immunodeficiency Disease (SCID)
Severe Combined Immunodeficiency Disease (SCID) RAG1 related
Skeletal Dysplasia 2 (SD2)
Spinal Dysraphism
Spondylocostal Dysostosis, Autosomal Recessive
Spongy Degeneration with Cerebella Ataxia Subtype 1, KCNJ10-related
Tail length, Short
Thrombopathia (CalDAG-GEFI)
Trapped Neutrophil Syndrome (TNS)
Tremor, X-linked
Vitamin D-resistant Rickets
Von Willebrand Disease I
Von Willebrand Disease II
Von Willebrand Disease III
X-linked Ectodermal Dysplasia
X-linked Severe Combined Immunodeficiency Disease (XSCID)
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