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.
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 |
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 |