Search for Animal Records


The OFA has health testing records on millions of individual dogs and cats.

This search function is for you to find records for specific animals or litters, breeds in general, or specific tests and conditions.

We have designed this search to help you find the information you are curious about.


Pick one of the search profiles below, then fill out what your know and are looking for.


SPECIFIC DOG/LITTER

Choose at least one of the following:
Registration # of dog/litter:

List of Registration Numbers:

One registration # per line. No punctuation.
Registered name/Kennel name:



CHIC/OFA #:

Partial OFA#s OK
e.g.: LR-EYE1234
Any additional filters:
Group:










Breed name:

Type at least 3 characters/pick from list
Sex:

Parent Registration #s:
(Sire)
(Dam)
Birth Year:

Type as 4-digits. e.g. 2012
(From)
(Thru)

or Age (now):


SPECIFIC BREED

Choose one breed:
Breed name:

Type at least 3 characters/pick from list
Any additional filters:
Birth Year:

Type as 4-digits. e.g. 2012
(From)
(Thru)

Age:


Reporting Year:








Testing Year:








Sex:

Special Programs:


SPECIFIC HEALTH TEST/DISORDER

Health Registry:
Choose one registry:


Type at least 3 characters to find.
Or filter above list by evaluation method:




Any additional filters:
Results:
Choose specific test/health registry
to see possible outcomes...
ADVANCED CARDIAC





























ACHROMATOPSIA DAY BLINDNESS





AVA ELBOWS

AGOUTI

































AVA HIPS

ALASKAN HUSKY ENCEPHALOPATHY



AMSTAFF LARYNGEAL PARALYSIS/POLYNEUROPATHY



ACRAL MUTILATION SYNDROME





ADULT ONSET NEUROPATHY





ARCH


AVA EYES

PROGRESSIVE RETINAL ATROPHY BBS2 VARIANT



BASIC CARDIAC















BVA ELBOWS

BVA HIPS

BENIGN FAMILIAL JUVENILE EPILEPSY





BAER HEARING TEST






BAER HEARING (ES)


BROWN (TYRP 1)




DTR BUFF





PRA-CRD4/CORD1



CONGENITAL CARDIAC



CEREBELLAR ATAXIA (CA1)



CATARACTS





CEREBELLAR DEGENERATION





COBALAMIN MALABSORPTION





CNS ATROPHY WITH CEREBELLAR ATAXIA



NEONATAL CEREBELLAR CORTICAL DEGENERATION





CANINE CYCLIC NEUTROPENIA





CONE DEGENERATION





PRA - CONE ROD DYSTROPHY 3





CONGENITAL DEAFNESS (DNA BASED)



CEREBELLAR DEGERATION-MYOSITITS COMPLEX (CDMC)



CHONDRODYSTROPHY (CDDY/IVDD)





COLLIE EYE ANOMALY





CONGENITAL EYE DISEASE



CONGENITAL HYPOTHROIDISM W/ GOITER





CANINE HEALTH

CHONDRODYSPLASIA (CDPA)





CONGENITAL IDIOPATHIC MEGAESOPHAGUS



CARDIOMYOPATHY AND JUVENILE MORTALITY



CEROID LIPOFUSCINOSIS







GOLDEN RETRIEVER NEURONAL CEROID LIPOFUSCINOSIS (NCL)





CANINE LEUKOCYTE ADHESION DEF.













CRANIOMANDIBULAR OSTEOPATHY





CANINE MULTIFOCAL RETINOPATHY





CONGENITAL MYASTHENIC SYNDROME





SKULL (DEPRECATED TEST)



CENTRONUCLEAR MYOPATHY





CALCIUM OXALATE BLADDER STONES





HEREDITARY CALCIUM OXALATE UROLITHIASIS










CLEFT PALATE





CLEFT LIP/PALATE SYNDACTYLY





CONE ROD DYSTROPHY 2



CONE ROD DYSTROPHY










COPPER TOXICOSIS

























COPPER TOXICOSIS - LIVER



CYSTINURIA






































DILUTION D2



DOBERMAN ALPHA-MANNOSIDOSIS (AMAN)



K LOCUS DATABASE








DAY BLINDNESS/RETINAL DEGENERATION





DILATED CARDIOMYOPATHY






















DISPROPORTIONATE DWARFISM



DNA DATA BANK



DENTITION






DRY EYE CURLY COAT SYNDROME





DEGENERATIVE ENCEPHALOPATHY





DHH DALMATION DATA BANK

D LOCUS





DEGENERATIVE MYELOPATHY











DEGENERATIVE MYELOPATHY B





DEGENERATIVE MYELOPATHY (DM) FLASH


DEGENERATIVE MYELOPATHY RISK MODIFIER



DERMATOMYOSITIS














































































DELAYED POSTOPERATIVE HEMORRHAGE (DEPOH)



DENTAL SKELETAL RETINAL ANOMALY



DOBERMAN VESTIBULAR OSTEOPATHY














DANDY WALKER-LIKE MALFORMATION SYNDROME





ECTODERMAL DYSPLASIA



EPISODIC FALLING





EPIDERMOLYTIC HYPERKERATOSIS



EXERCISE INDUCED COLLAPSE





ELBOW















HEREDITARY NECROTIZING MYELOPATHY





EARLY ONSET DEAFNESS



EARLY ONSET PRA





CERF


CERF-ABNORMAL

EARLY RETINAL DEGENERATION



EYES








Breeder Option(s)





































FACTOR VII DEFICIENCY





FANCONI SYNDROME









FUCOSIDOSIS



FACTOR XI DEFICIENCY





FAMILIAL ENAMEL HYPOPLASIA





INT'L ELBOW REGISTRY


INT'L HIP REGISTRY


FAMILIAL NEPHROPATHY





GLYCOGEN STORAGE DISEASE IIIA





GDC BAER HEARING


GLOBOID CELL LEUKODYSTROPHY



GRAY COLLIE SYNDROME





GDC ELBOWS



GDC HIPS







GM1-GANGLIOSIDOSIS





GM2-GANGLIOSIDOSIS





GONIOSCOPY





GR1 PROGRESSIVE RETINAL ATROPHY





GR2 PROGRESSIVE RETINAL ATROPHY





GLYCOGEN STORAGE DISEASE II



GDC SEBACEOUS ADENITIS



GSDCA TEMPERAMENT TEST

GLANZMANN'S THROMBASTHENIA





HEREDITARY CATARACTS





HIPS











HEREDITARY FOOTPAD HYPERKERATOSIS





HARLEQUIN


HEMOPHILIA A





HEMOPHILIA B





HEREDITARY NEPHRITIS





HEREDITARY NASAL PARAKERATOSIS





HOLTER ANECDOTAL INFORMATION



HISTIOCYTIC SARCOMA PRE-TEST SH




HYPERURICOSURIA





HYPOMYELINATION





ICHTHYOSIS ICH2





ICHTHYOSIS 3 (ICH3)




INTERNATIONAL CARDIAC EXAM


ICHTHYOSIS





INT'L CLAD EXAM

IRISH SETTER GENETIC REGISTRY




IMERSLUND-GRASBECK SYNDROME





INHERITED MYOPATHY



INFLAMMATORY MYOPATHY (MYOSITIS)





INT'L OPHTHALMOLOGICAL EXAM




CHONDRODYSPLASIA (ITGA10, KBD/NE TYPE)



INHERITED VENTRICULAR ARRHYTHMIA



JUVENILE ADDISON'S DISEASE





JUVENILE DILATED CARDIOMYOPATHY











JUVENILE MYOCLONIC EPILEPSY





JUVENILE CATARACTS (D)





KIDNEY


L 2 HYDROXYGLUTARIC ACIDUREA





LETHAL ACRODERMATITIS



LEUKOCYTE ADHESION DEFICIENCY





NEURONAL CEROID LIPOFUSCINOSIS AM BULLDOG TYPE (NCL 10)





LUPOID DERMATOSIS





LAFORA EPILEPSY










LEUKOENCEPHALOMYELOPATHY





LATE ONSET ATAXIA





LEGG-CALVE-PERTHES


LEONBERGER POLYNEUROPATHY 2





LEONBERGER POLYNEUROPATHY 3





LEONBERGER POLYNEUROPATHY 1





JUVENILE LARYNGEAL PARALYSIS & POLYNEUROPATHY (LPP)





LAGOTTO STORAGE DISEASE





NEURONAL CEROID LIPOFUSCINOSIS (TT)





LARYNGEAL PARALYSIS



MUCOPOLYSACCHARIDOSIS (MPS) IIIA





MUCOPOLYSACCHARIDOSIS (MPS) IIIB





MUCOPOLYSACCHARIDOSIS (MPS) VI





MUCOPOLYSACCHARIDOSIS (MPS) VII





MACROTHROMBOCYTOPENIA





MYCOBACTERIUM AVIAN COMPLEX





MIZZOU BIOMARKER STUDY

MYOTONIA CONGENITA





MCR1 (ELOCUS)








MACULAR CORNEAL DYSTROPHY





MAXILLARY CANINE-TOOTH MESIOVERSION



MUSCULAR DYSTROPHY






MULTIPLE DRUG RESISTANCE (MDR1)





MEDIUM CHAIN ACYL-COA DEHYDROGENASE DEFICIENCY (MCADD)



MUCOPOLYSACCHARIDOSIS I (MPS I)





MUSLADIN-LUEKE SYNDROME





MUCOPOLYSACCHARIDOSIS I



MERLE





MICROPHTHALMIA SYNDROME





MU DATABANK

NEUROAXONAL DYSTROPHY





NARCOLEPSY





NEONATAL CEREBELLAR ATAXIA





NEURONAL CEROID LIPOFUSCINOSIS
































NEURONAL DEGENERATION





NEONATAL ENCEPHALOPATHY





NEONATAL ENCEPHALOPATHY W/SEIZURES





NON-HSF4 CATARACTS



NECROTIZING MENINGOENCEPHALITIS



PRIMARY OPEN ANGLE GLAUCOMA



OSTEOCHONDRODYSPLASIA



OVC ELBOWS


OVC HIPS


OSTEOGENESIS IMPERFECTA



PRA TYPE 3





RCD4 PROGRESSIVE RETINAL ATROPHY





PROGRESSIVE RETINAL ATROPHY 5



PATELLA






PIEBALD/WHITE SPOTTING




PRIMARY CILIARY DYSKINESIA





PRIMARY CLOSED ANGLE GLAUCOMA



PITUITARY DWARFISM





PYRUVATE DEHYDROGENASE PHOSPHATASE DEFICIENCY





PERIANAL FISTULA



PHOSPHOFRUCTOKINASE DEFICIENCY





PRIMARY HYPEROXALURIA





PENNHIP HIPS


PRIMARY HYPERPARATHYROIDISM




PYRUVATE KINASE DEFICIENCY





POLYCYSTIC KIDNEY DISEASE



PRIMARY LENS LUXATION






PROTEIN LOSING NEPHROPATHY





POLYMYOSITIS




PERSISTENT MUELLERIAN DUCT SYNDROME





POLYNEUROPATHY





CANINE MULTIPLE SYSTEM DEGENERATION





PROGRESSIVE RETINAL ATROPHY
































































PAROXYSMAL DYSKINESIA





PRA - ROD CONE DYSPLASIA 3





RENAL DYSPLASIA (D)



RETINAL DYSPLASIA/OPTIC NERVE HYPOPLASIA



RETINAL DYSPLASIA /OSD





RFGS







RECEPTOR PLATELET DISORDER





ARRHYTHMOGENIC RIGHT VENTRICULAR CARDIOMYOPATHY















SEBACEOUS ADENITIS





SHAR-PEI AUTO-INFLAMMATORY DISEASE












SUBAORTIC STENOSIS (SAS)



SERUM BILE ACID



SPINOCEREBELLAR ATAXIA





SEVERE COMBINED IMMUNODEFICIENCY





SPINAL DYSRAPHISM





SKELETAL DYSPLASIA 2





SPONGY DEGENERATION WITH CEREBELLAR ATAXIA














STARGARDT DISEASE



SHOULDER





SIBERIAN HUSKY OPTH. REGISTRY

SIBERIAN HUSKY POLYNEUROPATHY





SPONGIFORM LEUKOENCEPHALOMYELOPATHY





SPINAL MUSCULAR ATROPHY (SMA)



SENSORY NEUROPATHY





STATIONARY NIGHT BLINDNESS





SPINE














SHAR-PEI PRIMARY OPEN ANGLE GLAUCOMA/PRIMARY LENS LUXATION



SUCCINIC SEMIALDEHYDE DEHYDROGENASE DEFICIENCY (SSADHD)





SIBERIAN HUSKY SHAKING PUPPY SYNDROME





STENOTIC NARES

CARDIAC LAMINOPATHY (CLAM)



THYROID







TRAPPED NEUTROPHIL SYNDROME





THROMBOPATHIA





TRACHEAL HYPOPLASIA







URINE NITROPRUSSIDE (CYSTINURIA)


VAN DEN ENDE-GUPTA SYNDROME



VON WILLEBRANDS





VON WILLEBRANDS CORNELL BLOOD ASSAY





GRFATHERED VON WILLEBRANDS DPCA



DPCA WAE




WCVM ELBOWS


WCVM HIPS


WHIPPET HEALTH FOUNDATION

WOLFHOUND STARTLE DISEASE





XANTHINURIA





X-LINKED MYOTUBULAR MYOPATHY



Reporting Year:








Testing Year:








Breed name:

Type at least 3 characters
Sex:

Birth Year:

Type as 4-digits. e.g. 2012
(From)
(Thru)

Age:


MARKED AS FAVORITES
Saved Application Numbers
QUICKSEARCH
Registration, Name, Litter, CHIC#:

Choose from the following:
Registration # of dog/litter:
List of Registration Numbers:

One registration # per line. No punctuation.
Registered name/Kennel name:



CHIC/OFA #:

Partial OFA#s OK
e.g.: LR-EYE1234
Special Programs:




Group:










Breed name:

Type at least 3 characters/pick from list
Birth Year:

Type as 4-digits. e.g. 2012
(From)
(Thru)

Or Age (now):


Sex:

Parent Registration #s:


Health Registry: (Hold Ctrl/Cmd key to select multiple)


Type at least 3 characters to find. Or filter above list by evaluation method:




Results:
Choose specific test/health registry
to see possible outcomes...
ADVANCED CARDIAC





























ACHROMATOPSIA DAY BLINDNESS





AVA ELBOWS

AGOUTI

































AVA HIPS

ALASKAN HUSKY ENCEPHALOPATHY



AMSTAFF LARYNGEAL PARALYSIS/POLYNEUROPATHY



ACRAL MUTILATION SYNDROME





ADULT ONSET NEUROPATHY





ARCH


AVA EYES

PROGRESSIVE RETINAL ATROPHY BBS2 VARIANT



BASIC CARDIAC















BVA ELBOWS

BVA HIPS

BENIGN FAMILIAL JUVENILE EPILEPSY





BAER HEARING TEST






BAER HEARING (ES)


BROWN (TYRP 1)




DTR BUFF





PRA-CRD4/CORD1



CONGENITAL CARDIAC



CEREBELLAR ATAXIA (CA1)



CATARACTS





CEREBELLAR DEGENERATION





COBALAMIN MALABSORPTION





CNS ATROPHY WITH CEREBELLAR ATAXIA



NEONATAL CEREBELLAR CORTICAL DEGENERATION





CANINE CYCLIC NEUTROPENIA





CONE DEGENERATION





PRA - CONE ROD DYSTROPHY 3





CONGENITAL DEAFNESS (DNA BASED)



CEREBELLAR DEGERATION-MYOSITITS COMPLEX (CDMC)



CHONDRODYSTROPHY (CDDY/IVDD)





COLLIE EYE ANOMALY





CONGENITAL EYE DISEASE



CONGENITAL HYPOTHROIDISM W/ GOITER





CANINE HEALTH

CHONDRODYSPLASIA (CDPA)





CONGENITAL IDIOPATHIC MEGAESOPHAGUS



CARDIOMYOPATHY AND JUVENILE MORTALITY



CEROID LIPOFUSCINOSIS







GOLDEN RETRIEVER NEURONAL CEROID LIPOFUSCINOSIS (NCL)





CANINE LEUKOCYTE ADHESION DEF.













CRANIOMANDIBULAR OSTEOPATHY





CANINE MULTIFOCAL RETINOPATHY





CONGENITAL MYASTHENIC SYNDROME





SKULL (DEPRECATED TEST)



CENTRONUCLEAR MYOPATHY





CALCIUM OXALATE BLADDER STONES





HEREDITARY CALCIUM OXALATE UROLITHIASIS










CLEFT PALATE





CLEFT LIP/PALATE SYNDACTYLY





CONE ROD DYSTROPHY 2



CONE ROD DYSTROPHY










COPPER TOXICOSIS

























COPPER TOXICOSIS - LIVER



CYSTINURIA






































DILUTION D2



DOBERMAN ALPHA-MANNOSIDOSIS (AMAN)



K LOCUS DATABASE








DAY BLINDNESS/RETINAL DEGENERATION





DILATED CARDIOMYOPATHY






















DISPROPORTIONATE DWARFISM



DNA DATA BANK



DENTITION






DRY EYE CURLY COAT SYNDROME





DEGENERATIVE ENCEPHALOPATHY





DHH DALMATION DATA BANK

D LOCUS





DEGENERATIVE MYELOPATHY











DEGENERATIVE MYELOPATHY B





DEGENERATIVE MYELOPATHY (DM) FLASH


DEGENERATIVE MYELOPATHY RISK MODIFIER



DERMATOMYOSITIS














































































DELAYED POSTOPERATIVE HEMORRHAGE (DEPOH)



DENTAL SKELETAL RETINAL ANOMALY



DOBERMAN VESTIBULAR OSTEOPATHY














DANDY WALKER-LIKE MALFORMATION SYNDROME





ECTODERMAL DYSPLASIA



EPISODIC FALLING





EPIDERMOLYTIC HYPERKERATOSIS



EXERCISE INDUCED COLLAPSE





ELBOW















HEREDITARY NECROTIZING MYELOPATHY





EARLY ONSET DEAFNESS



EARLY ONSET PRA





CERF


CERF-ABNORMAL

EARLY RETINAL DEGENERATION



EYES








Breeder Option(s)





































FACTOR VII DEFICIENCY





FANCONI SYNDROME









FUCOSIDOSIS



FACTOR XI DEFICIENCY





FAMILIAL ENAMEL HYPOPLASIA





INT'L ELBOW REGISTRY


INT'L HIP REGISTRY


FAMILIAL NEPHROPATHY





GLYCOGEN STORAGE DISEASE IIIA





GDC BAER HEARING


GLOBOID CELL LEUKODYSTROPHY



GRAY COLLIE SYNDROME





GDC ELBOWS



GDC HIPS







GM1-GANGLIOSIDOSIS





GM2-GANGLIOSIDOSIS





GONIOSCOPY





GR1 PROGRESSIVE RETINAL ATROPHY





GR2 PROGRESSIVE RETINAL ATROPHY





GLYCOGEN STORAGE DISEASE II



GDC SEBACEOUS ADENITIS



GSDCA TEMPERAMENT TEST

GLANZMANN'S THROMBASTHENIA





HEREDITARY CATARACTS





HIPS











HEREDITARY FOOTPAD HYPERKERATOSIS





HARLEQUIN


HEMOPHILIA A





HEMOPHILIA B





HEREDITARY NEPHRITIS





HEREDITARY NASAL PARAKERATOSIS





HOLTER ANECDOTAL INFORMATION



HISTIOCYTIC SARCOMA PRE-TEST SH




HYPERURICOSURIA





HYPOMYELINATION





ICHTHYOSIS ICH2





ICHTHYOSIS 3 (ICH3)




INTERNATIONAL CARDIAC EXAM


ICHTHYOSIS





INT'L CLAD EXAM

IRISH SETTER GENETIC REGISTRY




IMERSLUND-GRASBECK SYNDROME





INHERITED MYOPATHY



INFLAMMATORY MYOPATHY (MYOSITIS)





INT'L OPHTHALMOLOGICAL EXAM




CHONDRODYSPLASIA (ITGA10, KBD/NE TYPE)



INHERITED VENTRICULAR ARRHYTHMIA



JUVENILE ADDISON'S DISEASE





JUVENILE DILATED CARDIOMYOPATHY











JUVENILE MYOCLONIC EPILEPSY





JUVENILE CATARACTS (D)





KIDNEY


L 2 HYDROXYGLUTARIC ACIDUREA





LETHAL ACRODERMATITIS



LEUKOCYTE ADHESION DEFICIENCY





NEURONAL CEROID LIPOFUSCINOSIS AM BULLDOG TYPE (NCL 10)





LUPOID DERMATOSIS





LAFORA EPILEPSY










LEUKOENCEPHALOMYELOPATHY





LATE ONSET ATAXIA





LEGG-CALVE-PERTHES


LEONBERGER POLYNEUROPATHY 2





LEONBERGER POLYNEUROPATHY 3





LEONBERGER POLYNEUROPATHY 1





JUVENILE LARYNGEAL PARALYSIS & POLYNEUROPATHY (LPP)





LAGOTTO STORAGE DISEASE





NEURONAL CEROID LIPOFUSCINOSIS (TT)





LARYNGEAL PARALYSIS



MUCOPOLYSACCHARIDOSIS (MPS) IIIA





MUCOPOLYSACCHARIDOSIS (MPS) IIIB





MUCOPOLYSACCHARIDOSIS (MPS) VI





MUCOPOLYSACCHARIDOSIS (MPS) VII





MACROTHROMBOCYTOPENIA





MYCOBACTERIUM AVIAN COMPLEX





MIZZOU BIOMARKER STUDY

MYOTONIA CONGENITA





MCR1 (ELOCUS)








MACULAR CORNEAL DYSTROPHY





MAXILLARY CANINE-TOOTH MESIOVERSION



MUSCULAR DYSTROPHY






MULTIPLE DRUG RESISTANCE (MDR1)





MEDIUM CHAIN ACYL-COA DEHYDROGENASE DEFICIENCY (MCADD)



MUCOPOLYSACCHARIDOSIS I (MPS I)





MUSLADIN-LUEKE SYNDROME





MUCOPOLYSACCHARIDOSIS I



MERLE





MICROPHTHALMIA SYNDROME





MU DATABANK

NEUROAXONAL DYSTROPHY





NARCOLEPSY





NEONATAL CEREBELLAR ATAXIA





NEURONAL CEROID LIPOFUSCINOSIS
































NEURONAL DEGENERATION





NEONATAL ENCEPHALOPATHY





NEONATAL ENCEPHALOPATHY W/SEIZURES





NON-HSF4 CATARACTS



NECROTIZING MENINGOENCEPHALITIS



PRIMARY OPEN ANGLE GLAUCOMA



OSTEOCHONDRODYSPLASIA



OVC ELBOWS


OVC HIPS


OSTEOGENESIS IMPERFECTA



PRA TYPE 3





RCD4 PROGRESSIVE RETINAL ATROPHY





PROGRESSIVE RETINAL ATROPHY 5



PATELLA






PIEBALD/WHITE SPOTTING




PRIMARY CILIARY DYSKINESIA





PRIMARY CLOSED ANGLE GLAUCOMA



PITUITARY DWARFISM





PYRUVATE DEHYDROGENASE PHOSPHATASE DEFICIENCY





PERIANAL FISTULA



PHOSPHOFRUCTOKINASE DEFICIENCY





PRIMARY HYPEROXALURIA





PENNHIP HIPS


PRIMARY HYPERPARATHYROIDISM




PYRUVATE KINASE DEFICIENCY





POLYCYSTIC KIDNEY DISEASE



PRIMARY LENS LUXATION






PROTEIN LOSING NEPHROPATHY





POLYMYOSITIS




PERSISTENT MUELLERIAN DUCT SYNDROME





POLYNEUROPATHY





CANINE MULTIPLE SYSTEM DEGENERATION





PROGRESSIVE RETINAL ATROPHY
































































PAROXYSMAL DYSKINESIA





PRA - ROD CONE DYSPLASIA 3





RENAL DYSPLASIA (D)



RETINAL DYSPLASIA/OPTIC NERVE HYPOPLASIA



RETINAL DYSPLASIA /OSD





RFGS







RECEPTOR PLATELET DISORDER





ARRHYTHMOGENIC RIGHT VENTRICULAR CARDIOMYOPATHY















SEBACEOUS ADENITIS





SHAR-PEI AUTO-INFLAMMATORY DISEASE












SUBAORTIC STENOSIS (SAS)



SERUM BILE ACID



SPINOCEREBELLAR ATAXIA





SEVERE COMBINED IMMUNODEFICIENCY





SPINAL DYSRAPHISM





SKELETAL DYSPLASIA 2





SPONGY DEGENERATION WITH CEREBELLAR ATAXIA














STARGARDT DISEASE



SHOULDER





SIBERIAN HUSKY OPTH. REGISTRY

SIBERIAN HUSKY POLYNEUROPATHY





SPONGIFORM LEUKOENCEPHALOMYELOPATHY





SPINAL MUSCULAR ATROPHY (SMA)



SENSORY NEUROPATHY





STATIONARY NIGHT BLINDNESS





SPINE














SHAR-PEI PRIMARY OPEN ANGLE GLAUCOMA/PRIMARY LENS LUXATION



SUCCINIC SEMIALDEHYDE DEHYDROGENASE DEFICIENCY (SSADHD)





SIBERIAN HUSKY SHAKING PUPPY SYNDROME





STENOTIC NARES

CARDIAC LAMINOPATHY (CLAM)



THYROID







TRAPPED NEUTROPHIL SYNDROME





THROMBOPATHIA





TRACHEAL HYPOPLASIA







URINE NITROPRUSSIDE (CYSTINURIA)


VAN DEN ENDE-GUPTA SYNDROME



VON WILLEBRANDS





VON WILLEBRANDS CORNELL BLOOD ASSAY





GRFATHERED VON WILLEBRANDS DPCA



DPCA WAE




WCVM ELBOWS


WCVM HIPS


WHIPPET HEALTH FOUNDATION

WOLFHOUND STARTLE DISEASE





XANTHINURIA





X-LINKED MYOTUBULAR MYOPATHY



Reporting Year:








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