ALPACA

·  ATRESIA ANI

ANTELOPE

·  GOITRE, FAMILIAL

·  SPONGIFORM ENCEPHALOPATHY

AOUDAD

·  BLOOD GROUP SYSTEM A

·  BLOOD GROUP SYSTEM B

·  BLOOD GROUP SYSTEM C

·  BLOOD GROUP SYSTEM D

·  BLOOD GROUP SYSTEM F30

·  BLOOD GROUP SYSTEM F41

·  BLOOD GROUP SYSTEM M

·  BLOOD GROUP SYSTEM R

APE

·  BLOOD GROUP SYSTEM

ARGALI

·  INTERSEX

AUROCH

·  BLOOD GROUP SYSTEM

BABOON

·  BLOOD GROUP SYSTEM ABO

BAT

·  AMYLOIDOSIS, AA

BLACK

·  GOITRE, FAMILIAL in

BROWN

·  COAT COLOUR, ALBINISM in

BIGHORN

·  BLOOD GROUP SYSTEM

·  FREEMARTIN

·  HORNS

·  INTERSEX

BUDGERIGAR

·  CREST

·  FEATHER COLOUR

BUFFALO

·  ABOMASUM, DISPLACED

·  ACHONDROPLASIA

·  COAT COLOUR

·  DICEPHALUS

·  EPITHELIOGENESIS IMPERFECTA

·  EYE DEFECTS

·  FRAGILE X

·  FREEMARTIN

·  GOITRE, FAMILIAL

·  HERNIA, DIAPHRAGMATIC

·  INTERSEX

·  MICROPHTHALMIA

·  REVIEW

·  SCHISTOSOMUS REFLEXUS

·  SUPRABASILAR ACANTHOLYTIC MECHANOBULLOUS DERMATITIS

·  TWINNING, CONJOINED

RIVER

·  GENETIC MAPS in

·  SPONGIFORM ENCEPHALOPATHY in

WATER

·  COAT COLOUR in

·  COAT COLOUR, ALBINISM in

·  COAT COLOUR, WHITE in

·  EYE COLOUR in

·  HORN SHAPE in

·  HORNS in

·  VITILIGO in

CAMEL

·  BLOOD GROUP SYSTEM

·  CARDIOMYOPATHY, HYPERTROPHIC

·  CRYPTORCHIDISM

CARABAO

·  COAT COLOUR

CARP

·  SEX REVERSAL: XX MALE

GRASS

·  COAT COLOUR, ALBINISM in

CAT

·  ACHALASIA OF THE OESOPHAGUS, CONGENITAL

·  ACHONDROPLASIA

·  ACROMEGALY

·  ALLOIMMUNE HAEMOLYTIC ANAEMIA OF THE NEWBORN

·  ALOPECIA

·  AMYLOIDOSIS

·  AMYLOIDOSIS, AA

·  AMYLOIDOSIS, LAMBDA

·  AMYLOIDOSIS, RENAL

·  ANKYLOSIS, GENERALISED

·  ANODONTIA

·  AORTICOPULMONARY SEPTAL DEFECT

·  ARTHRITIS

·  ATAXIA

·  ATAXIA, CEREBELLAR

·  ATOPY

·  ATRESIA ANI

·  ATRESIA COLI

·  ATRIAL SEPTAL DEFECT

·  AUTOIMMUNE THROMBOCYTOPENIA

·  AUTOIMMUNE THYROIDITIS, SPONTANEOUS

·  AXONOPATHY, DISTAL

·  AXONOPATHY, PERIPHERAL

·  BLEEDING DISORDER

·  BLOOD GROUP SYSTEM

·  BLOOD GROUP SYSTEM AB

·  BONE LESION

·  BRACHYCEPHALIC AIRWAY OBSTRUCTION SYNDROME

·  BRACHYDACTYLY

·  BUDD-CHIARI SYNDROME

·  CARDIAC ANOMALY

·  CARDIOMYOPATHY

·  CARDIOMYOPATHY, DILATED

·  CARDIOMYOPATHY, HYPERTROPHIC

·  CATARACT

·  CATNIP RESPONSE

·  CEREBELLAR ABIOTROPHY

·  CEREBELLAR CORTICAL ATROPHY

·  CEREBELLAR DEGENERATION

·  CEREBELLAR HYPOPLASIA

·  CEREBELLAR MALFORMATION

·  CEROID LIPOFUSCINOSIS

·  CHEDIAK-HIGASHI SYNDROME

·  CHONDRODYSPLASIA

·  CLEFT PALATE

·  COAT COLOUR

·  COAT COLOUR, ALBINISM

·  COAT COLOUR, ALBINISM, OCULOCUTANEOUS TYPE I, TEMPERATURE-SENSITIVE

·  COAT COLOUR, GLITTER

·  COAT COLOUR, ORANGE

·  COAT COLOUR, PINK-EYED DILUTION

·  COAT COLOUR, WHITE

·  COAT COLOUR, WHITE SPOTTING

·  COLOBOMA

·  CONTACT ACTIVATION DEFECT

·  CORNEAL DYSTROPHY

·  COXOFEMORAL LUXATION

·  CRANIOSCHISIS

·  CRYPTORCHIDISM

·  CURL

·  CUSHING DISEASE

·  CYCLOPIA

·  CYSTIC LIVER

·  CYSTINURIA

·  DANDY-WALKER SYNDROME

·  DEAFNESS

·  DERMOID, NASAL, CONGENITAL

·  DERMOID, OCULAR, CONGENITAL

·  DIABETES

·  DIABETES INSIPIDUS

·  DIABETES MELLITUS

·  DIABETES MELLITUS, HYPEROSMOLAR NONKETOTIC

·  DIABETES MELLITUS, TYPE I

·  DIABETES MELLITUS, TYPE II

·  DICEPHALUS

·  DIPROSPUS

·  DWARFISM

·  DYSAUTONOMIA

·  EARS, FOLDED

·  EARS, FOUR

·  ECTRODACTYLY

·  EHLERS-DANLOS SYNDROME

·  EHLERS-DANLOS SYNDROME, TYPE VII

·  ELBOW LUXATION

·  ENCEPHALOMYELOPATHY

·  EPIDERMOLYSIS BULLOSA, DYSTROPHIC

·  EPILEPSY

·  EPISTAXIS

·  EPITHELIOGENESIS IMPERFECTA

·  ERYTHROCYTOSIS

·  EXENCEPHALY

·  EYE COLOUR

·  EYELID GLAND, THIRD, PROLAPSE OF

·  FACTOR X DEFICIENCY

·  FACTOR XI DEFICIENCY

·  FACTOR XII DEFICIENCY

·  FIBRODYSPLASIA OSSIFICANS

·  FRAGILE SITE

·  FUCOSIDOSIS, ALPHA

·  GANGLIOSIDOSIS

·  GANGLIOSIDOSIS, GM1

·  GANGLIOSIDOSIS, GM2

·  GENETIC MAPS

·  GLAUCOMA

·  GLOMERULONEPHRITIS

·  GLUCOSE-6-PHOSPHATE DEHYDROGENASE DEFICIENCY

·  GLYCOGEN STORAGE DISEASE II

·  GLYCOGEN STORAGE DISEASE IV

·  GOITRE, FAMILIAL

·  HAEMOLYTIC ANAEMIA, AUTOIMMUNE

·  HAEMOPHAGOCYTIC SYNDROME

·  HAEMOPHILIA A

·  HAEMOPHILIA B

·  HAIR LENGTH

·  HEART DEFECT, CONGENITAL

·  HERNIA

·  HERNIA, DIAPHRAGMATIC

·  HERNIA, HIATAL

·  HERNIA, INGUINAL

·  HERNIA, PERITONEOPERICARDIAL

·  HERNIA, UMBILICAL

·  HIND LIMB PARALYSIS

·  HIP DYSPLASIA

·  HORNER SYNDROME

·  HYDROCEPHALUS

·  HYPERADRENOCORTICISM

·  HYPERALDOSTERONISM

·  HYPERBILIRUBINAEMIA, UNCLASSIFIED

·  HYPEREOSINOPHILIC SYNDROME

·  HYPERLIPOPROTEINAEMIA

·  HYPERPARATHYROIDISM

·  HYPERTENSION

·  HYPERTHYROIDISM

·  HYPERTRIGLYCERIDAEMIA

·  HYPOADRENOCORTICISM

·  HYPOMYELINATION OF THE CENTRAL NERVOUS SYSTEM

·  HYPOPARATHYROIDISM

·  HYPOPHOSPHATAEMIA

·  HYPOTHYROIDISM

·  HYPOTHYROIDISM, PRIMARY

·  HYPOTRICHOSIS

·  HYPOTRICHOSIS WITH THYMIC APLASIA, CONGENITAL

·  IMMUNODEFICIENCY

·  INTERSEX

·  INTESTINAL COBALAMIN MALABSORPTION

·  INTUSSUSCEPTION

·  IRIS DEFECTS

·  KARTAGENER SYNDROME

·  KRABBE DISEASE

·  LENS LUXATION

·  LIPIDOSIS

·  LIPIDOSIS, HEPATIC

·  LYSOSOMAL STORAGE DISEASE

·  MALIGNANT HYPERTHERMIA

·  MANNOSIDOSIS, ALPHA

·  MEGACOLON

·  MEGAOESOPHAGUS

·  METABOLIC DISORDER

·  METHAEMOGLOBINAEMIA

·  MITRAL VALVE STENOSIS

·  MONORCHIDISM

·  MUCOLIPIDOSIS II

·  MUCOPOLYSACCHARIDOSIS I

·  MUCOPOLYSACCHARIDOSIS VI

·  MUCOPOLYSACCHARIDOSIS VII

·  MUSCULAR DYSTROPHY

·  MUSCULAR DYSTROPHY, DUCHENNE AND BECKER TYPES

·  MYASTHENIA GRAVIS

·  MYCOSIS FUNGOIDES

·  MYELOCELE

·  MYOPATHY

·  MYOTONIA

·  NEPHROLITHIASIS

·  NEUROAXONAL DYSTROPHY

·  NIEMANN-PICK DISEASE, TYPE C

·  OCULAR DISEASE

·  OLIVO-PONTO-CEREBELLAR HYPOPLASIA

·  OMPHALOCELE

·  ORCHITIS

·  OSTEOARTHRITIS

·  OSTEOCHONDRODYSPLASIA

·  OSTEODYSTROPHY

·  OSTEOGENESIS IMPERFECTA

·  OTITIS EXTERNA, SUSCEPTIBILITY TO

·  OTITIS MEDIA, SUSCEPTIBILITY TO

·  OVARIAN DYSGENESIS

·  OXALOSIS II

·  PANCREATIC INSUFFICIENCY, EXOCRINE

·  PATELLAR LUXATION

·  PATENT DUCTUS ARTERIOSUS

·  PATENT URACHUS

·  PELGER-HUET ANOMALY

·  PEMPHIGUS

·  PEROMELUS ASCELUS

·  PERSISTENT MULLERIAN DUCT SYNDROME

·  PERSISTENT RIGHT AORTIC ARCH

·  PERSISTENT TRUNCUS ARTERIOSUS

·  PERSISTENT URACHUS

·  PHEOCHROMOCYTOMA

·  POLYARTHRITIS

·  POLYCYSTIC KIDNEY DISEASE

·  POLYCYTHEMIA

·  POLYDACTYLY

·  POLYNEUROPATHY

·  PORPHYRIA, UNCLASSIFIED

·  PORTOSYSTEMIC SHUNT

·  PRIAPISM

·  PRIMARY SEBORRHEA-OLEOSA

·  PROGRESSIVE RETINAL ATROPHY

·  PYLORIC STENOSIS

·  RECTOVAGINAL FISTULA

·  RENAL DISEASE

·  RENAL HYPOPLASIA

·  RETINAL DEGENERATION

·  RETINAL DEGENERATION II

·  RETINAL DEGENERATION, CENTRAL

·  RETINAL DYSTROPHY

·  RETINITIS PIGMENTOSA, PERIPHERIN-RELATED

·  REVIEW

·  ROD-CONE DEGENERATION

·  ROD-CONE DYSPLASIA

·  SACRAL DYSGENESIS

·  SACRO-COCCYGEAL AGENESIS

·  SEPTAL DEFECT

·  SEX REVERSAL

·  SHOULDER LUXATION

·  SITUS INVERSUS

·  SPASTIC SYNDROME

·  SPINA BIFIDA

·  SPINA BIFIDA OCCULTA

·  SPINA BIFIDA WITH RADUSCHISIS

·  SPINAL DYSPLASIA

·  SPLIT HAND

·  SPONDYLOSIS DEFORMANS

·  SPONGIFORM ENCEPHALOPATHY

·  STRABISMUS

·  SUBAORTIC STENOSIS

·  SUBVALVULAR PULMONARY STENOSIS

·  SUPRAVALVULAR AORTIC STENOSIS

·  SYNDACTYLY

·  SYRINGOMYELIA

·  SYSTEMIC HYPERTENSION

·  SYSTEMIC LUPUS ERYTHEMATOSUS

·  TAIL, STUMP

·  TAILLESSNESS

·  TESTICULAR FEMINIZATION

·  TETRALOGY OF FALLOT

·  THIRD HIND LEG

·  THROMBOCYTOPAENIA

·  TREMOR

·  TRICUSPID STENOSIS

·  UROGENITAL AGENESIS, UNILATERAL

·  UROLITH, KMGP

·  UROLITHIASIS

·  URTICARIA PIGMENTOSA

·  VARIOUS DISORDERS

·  VENTRICULAR SEPTAL DEFECT

·  VERTEBRAL ANOMALIES

·  VISION, ABNORMAL

·  VISUAL PATHWAY, ABNORMAL

·  VITAMIN-K-DEPENDENT BLOOD COAGULATION FACTORS DEFICIENCY

·  WAARDENBURG SYNDROME

·  XANTHINURIA

CATTLE

·  ABOMASUM, DISPLACED

·  ABORTION

·  ABRACHIA

·  ACHONDROPLASIA

·  ACHONDROPLASIA FOETALIS

·  ACROTERIASIS CONGENITA

·  ADACTYLY

·  ADENOHYPOPHYSEAL APLASIA

·  AGENESIS OF CORPUS CALLOSUM

·  AGNATHIA

·  ALLERGIC RHINITIS

·  ALOPECIA

·  AMPUTATED

·  AMYLOIDOSIS, RENAL

·  ANENCEPHALY

·  ANHIDROTIC ECTODERMAL DYSPLASIA

·  ANKYLOSIS, GENERALISED

·  ANOPHTHALMOS

·  ANOPHTHALMOS MICROPHTHALMOS

·  APLASIA SEGMENTALIS DUCTUS WOLFFII

·  ARACHNOMELIA

·  ARNOLD-CHIARI MALFORMATION

·  ARTHROGRYPOSIS

·  ARTHROGRYPOSIS AND PALATOSCHISIS SYNDROME

·  ASCITES

·  ATAXIA

·  ATAXIA, CEREBELLAR

·  ATRESIA ANI

·  ATRESIA COLI

·  ATRESIA ILEI

·  ATRESIA INTESTINAL

·  ATRIAL SEPTAL DEFECT

·  ATROPHIC RHINITIS

·  AXONOPATHY

·  BLACK HAIR FOLLICLE DYSPLASIA

·  BLEEDING DIATHESIS

·  BLEEDING DISORDER

·  BLOOD GROUP SYSTEM

·  BLOOD GROUP SYSTEM B

·  BLOOD GROUP SYSTEM C

·  BLOOD GROUP SYSTEM J

·  BLOOD GROUP SYSTEM L

·  BLOOD GROUP SYSTEM M

·  BLOOD GROUP SYSTEM S

·  BRACHYGNATHIA

·  BRACHYGNATHIA SUPERIOR

·  BRACHYGNATHIA SUPERIOR AND DEGENERATIVE JOINT DISEASE

·  BRACHYSPINA

·  CARDIAC ANOMALY

·  CARDIOMYOPATHY

·  CARDIOMYOPATHY AND WOOLLY HAIRCOAT SYNDROME

·  CARDIOMYOPATHY, DILATED

·  CARDIOMYOPATHY, HYPERTROPHIC

·  CATARACT

·  CEREBELLAR CORTICAL ATROPHY

·  CEREBELLAR DISEASE

·  CEREBELLAR HYPOPLASIA

·  CEROID LIPOFUSCINOSIS

·  CHEDIAK-HIGASHI SYNDROME

·  CHONDRODYSPLASIA

·  CHONDRODYSTROPHY

·  CHRONIC INTERSTITIAL NEPHRITIS WITH DIFFUSE ZONAL FIBROSIS

·  CITRULLINAEMIA

·  CLAW DEFECTS

·  CLEFT PALATE

·  COAT COLOUR

·  COAT COLOUR, AGOUTI

·  COAT COLOUR, ALBINISM

·  COAT COLOUR, ALBINISM, INCOMPLETE

·  COAT COLOUR, BROWN

·  COAT COLOUR, DOMINANT WHITE

·  COAT COLOUR, EXTENSION

·  COAT COLOUR, ROAN

·  COAT COLOUR, SPOTTED

·  COLOBOMA

·  COMPLEX VERTEBRAL MALFORMATION

·  CONGENITAL ANAEMIA, DYSKERATOSIS AND PROGRESSIVE ALOPECIA

·  CONGENITAL JOINT LAXITY AND DWARFISM

·  CONVULSIONS AND ATAXIA, FAMILIAL

·  CORKSCREW PENIS

·  CORNEAL CLOUDING

·  CORNEAL OPACITY

·  CRANIAL DUPLICATION

·  CRANIOSCHISIS

·  CRYPTORCHIDISM

·  CURLY COAT

·  CURLY HAIR, KARAKUL-TYPE

·  CYCLOPIA

·  CYSTIC OVARY

·  DEBILITY, CONGENITAL

·  DEFECTIVE KERATOGENESIS OF HOOVES AND MOUTH

·  DEFICIENCY OF URIDINE MONOPHOSPHATE SYNTHASE

·  DERMOID, OCULAR, CONGENITAL

·  DIABETES MELLITUS

·  DIABETES MELLITUS, TYPE I

·  DIPROSPUS

·  DODDLER

·  DOUBLE CERVIX

·  DUCK-LEGGED

·  DUPLICATION OF CERVIX

·  DUPLICATION OF OS UTERI

·  DWARFISM

·  DWARFISM, DEXTER

·  DWARFISM, LARON

·  DWARFISM, CHONDRODYSTROPHY

·  DWARFISM, CHONDROPLASTIC

·  DWARFISM, GROWTH-HORMONE-RECEPTOR DEFICIENCY

·  DWARFISM, PROPORTIONAL

·  DWARFISM, PROPORTIONATE

·  DWARFISM, SNORTER

·  DWARFISM, STUMPY

·  DWARFISN, SNORTER

·  DYSERYTHROPOIESIS

·  EARS, CROP

·  EARS, DOUBLE

·  EARS, NOTCHED

·  ECTRODACTYLY

·  ECTROMELIA

·  EHLERS-DANLOS SYNDROME

·  EHLERS-DANLOS SYNDROME, TYPE VII

·