CARP

·  SEX REVERSAL: XX MALE

CAT

·  CARDIOMYOPATHY, HYPERTROPHIC

·  CEREBELLAR DEGENERATION

·  CEROID LIPOFUSCINOSIS

·  CHEDIAK-HIGASHI SYNDROME

·  COAT COLOUR, ALBINISM

·  COAT COLOUR, ORANGE

·  EHLERS-DANLOS SYNDROME

·  EHLERS-DANLOS SYNDROME, TYPE VII

·  EPITHELIOGENESIS IMPERFECTA

·  FACTOR XII DEFICIENCY

·  FUCOSIDOSIS, ALPHA

·  GANGLIOSIDOSIS, GM1

·  GANGLIOSIDOSIS, GM2

·  GLUCOSE-6-PHOSPHATE DEHYDROGENASE DEFICIENCY

·  GLYCOGEN STORAGE DISEASE II

·  GLYCOGEN STORAGE DISEASE IV

·  HAEMOPHILIA A

·  HAEMOPHILIA B

·  HAIR LENGTH

·  HYPERLIPOPROTEINAEMIA

·  KRABBE DISEASE

·  MANNOSIDOSIS, ALPHA

·  MUCOLIPIDOSIS II

·  MUCOPOLYSACCHARIDOSIS I

·  MUCOPOLYSACCHARIDOSIS VI

·  MUCOPOLYSACCHARIDOSIS VII

·  MUSCULAR DYSTROPHY, DUCHENNE AND BECKER TYPES

·  NIEMANN-PICK DISEASE, TYPE C

·  OSTEOCHONDRODYSPLASIA

·  OSTEODYSTROPHY

·  OXALOSIS II

·  POLYCYSTIC KIDNEY DISEASE

·  PORPHYRIA, UNCLASSIFIED

·  RETINAL DEGENERATION II

·  ROD-CONE DYSPLASIA

·  TAILLESSNESS

·  TESTICULAR FEMINIZATION

·  VITAMIN-K-DEPENDENT BLOOD COAGULATION FACTORS DEFICIENCY

CATTLE

·  ANHIDROTIC ECTODERMAL DYSPLASIA

·  CARDIOMYOPATHY

·  CARDIOMYOPATHY, DILATED

·  CEROID LIPOFUSCINOSIS

·  CHEDIAK-HIGASHI SYNDROME

·  CHONDRODYSPLASIA

·  CHRONIC INTERSTITIAL NEPHRITIS WITH DIFFUSE ZONAL FIBROSIS

·  CITRULLINAEMIA

·  COAT COLOUR, AGOUTI

·  COAT COLOUR, ALBINISM

·  COAT COLOUR, BROWN

·  COAT COLOUR, DOMINANT WHITE

·  COAT COLOUR, EXTENSION

·  COAT COLOUR, ROAN

·  COAT COLOUR, SPOTTED

·  COMPLEX VERTEBRAL MALFORMATION

·  DEFICIENCY OF URIDINE MONOPHOSPHATE SYNTHASE

·  DWARFISM, DEXTER

·  DWARFISM, GROWTH-HORMONE-RECEPTOR DEFICIENCY

·  DWARFISM, SNORTER

·  DYSERYTHROPOIESIS

·  EHLERS-DANLOS SYNDROME

·  EHLERS-DANLOS SYNDROME, TYPE VII

·  EPITHELIOGENESIS IMPERFECTA

·  FACTOR XI DEFICIENCY

·  GANGLIOSIDOSIS, GM1

·  GLYCOGEN STORAGE DISEASE II

·  GLYCOGEN STORAGE DISEASE V

·  GOITRE, FAMILIAL

·  HORNS

·  HYPERBILIRUBINAEMIA, UNCLASSIFIED

·  HYPOTRICHOSIS

·  LETHAL TRAIT A46

·  LEUKOCYTE ADHESION DEFICIENCY

·  MANNOSIDOSIS, ALPHA

·  MANNOSIDOSIS, BETA

·  MAPLE SYRUP URINE DISEASE

·  MUCOPOLYSACCHARIDOSIS I

·  MUSCULAR HYPERTROPHY

·  MYOCLONUS

·  PORPHYRIA, CONGENITAL ERYTHROPOIETIC

·  PROGRESSIVE DEGENERATIVE MYELOENCEPHALOPATHY

·  PROTAMINE-2 DEFICIENCY

·  PROTOPORPHYRIA

·  RENAL DYSPLASIA

·  SEX REVERSAL: XY FEMALE

·  SPASTIC LETHAL

·  SPHEROCYTOSIS

·  SPINAL DYSMYELINATION

·  SPINAL MUSCULAR ATROPHY

·  SYNDACTYLY

·  TESTICULAR FEMINIZATION

·  TESTICULAR HYPOPLASIA

·  TIBIAL HEMIMELIA

·  TRIMETHYLAMINURIA

·  VERTICAL FIBRE HIDE DEFECT

CHICKEN

·  ACHONDROPLASIA, CREEPER

·  ACHROMATOSIS

·  AMETAPODIA

·  ANALPHALIPOPROTEINAEMIA

·  BALDNESS, CONGENITAL

·  BARRING

·  BLASTODERM DEGENERATION

·  BLUE EGGSHELL

·  COAT COLOUR, ALBINISM

·  COLOBOMA

·  CREST

·  DIPLOPODIA

·  DIPLOPODIA-2

·  DIPLOPODIA-3

·  DIPLOPODIA-4

·  DIPLOPODIA-5

·  DWARFISM, AUTOSOMAL

·  DWARFISM, CROOKED NECK

·  DWARFISM, SEX-LINKED

·  ENDOGENOUS VIRAL ELEMENT 1

·  EPILEPSY

·  EUMELANIN DILUTION BLUE

·  EUMELANIN EXTENSION

·  EUMELANIN RESTRICTOR

·  EXTENDED BLACK

·  FADED SHAKER

·  FEATHER COLOUR, ALBINISM

·  FEATHER COLOUR, ALBINISM, SEX-LINKED, IMPERFECT

·  FEATHER COLOUR, CHOCOLATE

·  FEATHER COLOUR, RECESSIVE WHITE

·  FEATHER COLOUR, SILVER

·  FEATHER CURLING

·  FEATHERING, Z-LINKED

·  FRIZZLE

·  HENNY FEATHERING

·  LADYKILLER

·  LIMBLESS

·  MICROMELIC SYNDROME

·  MUSCULAR DYSTROPHY

·  NAKED NECK

·  NANOMELIA

·  PAROXYSM

·  PEA COMB

·  PEROSIS

·  PLUMAGE PATTERN

·  POLYDACTYLY

·  POP-EYE

·  PRENATAL

·  PROTOPORPHYRIA

·  RESISTANCE TO AVIAN SARCOMA AND LEUKOSIS VIRUSES, SUBGROUP A

·  RESISTANCE TO AVIAN SARCOMA AND LEUKOSIS VIRUSES, SUBGROUP B

·  RESTRICTED OVULATOR

·  RETINAL DEGENERATION I

·  RIBOFLAVINURIA

·  RIBOSOMAL DNA DEFICIENCY

·  ROSE COMB

·  SCALELESS

·  SPERM DEGENERATION

·  TALPID-2

·  TALPID-3

·  VISUAL IMPAIRMENT

·  WHITE SKIN

·  WINGLESS

CONDOR

·  CHONDRODYSTROPHY

DOG

·  AFIBRINOGENAEMIA

·  ANHIDROTIC ECTODERMAL DYSPLASIA

·  BLACK HAIR FOLLICLE DYSPLASIA

·  BLOOD GROUP SYSTEM RH

·  C3 DEFICIENCY

·  CARDIOMYOPATHY, DILATED

·  CARPAL SUBLUXATION

·  CATARACT

·  CEROID LIPOFUSCINOSIS

·  CEROID LIPOFUSCINOSIS, JUVENILE ONSET

·  COAT COLOUR

·  COAT COLOUR, ALBINISM

·  COAT COLOUR, BROWN

·  COAT COLOUR, EXTENSION

·  COAT COLOUR, MERLE

·  CYSTINURIA

·  DEAFNESS

·  DERMATOFIBROSIS

·  DWARFISM, HYPOCHONDROPLASTIC

·  DWARFISM, PITUITARY

·  EHLERS-DANLOS SYNDROME

·  EPIDERMOLYSIS BULLOSA, DYSTROPHIC

·  EPILEPSY

·  FACTOR VII DEFICIENCY

·  FACTOR X DEFICIENCY

·  FACTOR XI DEFICIENCY

·  FACTOR XII DEFICIENCY

·  FUCOSIDOSIS, ALPHA

·  GANGLIOSIDOSIS, GM1

·  GANGLIOSIDOSIS, GM2

·  GAUCHER DISEASE, TYPE I

·  GLUTEN-SENSITIVE ENTEROPATHY

·  GLYCOGEN STORAGE DISEASE I

·  GLYCOGEN STORAGE DISEASE II

·  GLYCOGEN STORAGE DISEASE VII

·  GONIODYSPLASIA, MESODERMAL

·  HAEMOPHILIA A

·  HAEMOPHILIA B

·  HYPERKERATOSIS, PALMOPLANTAR

·  HYPOCATALASIA

·  HYPOPROTHROMBINAEMIA

·  HYPOTRICHOSIS

·  INTESTINAL COBALAMIN MALABSORPTION

·  KARTAGENER SYNDROME

·  KRABBE DISEASE

·  LEGG-CALVE-PERTHES DISEASE

·  LEUKOCYTE ADHESION DEFICIENCY

·  MALIGNANT HYPERTHERMIA

·  MENKES SYNDROME

·  MUCOPOLYSACCHARIDOSIS I

·  MUCOPOLYSACCHARIDOSIS II

·  MUCOPOLYSACCHARIDOSIS IIIA

·  MUCOPOLYSACCHARIDOSIS VI

·  MUCOPOLYSACCHARIDOSIS VII

·  MUSCULAR DYSTROPHY

·  MUSCULAR DYSTROPHY, DUCHENNE AND BECKER TYPES

·  MYASTHENIA GRAVIS

·  MYOCLONUS EPILEPSY OF LAFORA

·  MYOTONIA

·  NARCOLEPSY

·  NEPHRITIS, X-LINKED

·  NEPHRITIS, X-LINKED DOMINANT

·  NEPHRITIS, AUTOSOMAL DOMINANT

·  NEPHRITIS, AUTOSOMAL RECESSIVE

·  NEUTROPENIA, CYCLIC

·  NIEMANN-PICK DISEASE

·  OPTIC CHIASM, ABSENCE OF

·  OSTEOGENESIS IMPERFECTA

·  PRA-AUTOSOMAL DOMINANT

·  PRA-ROD-CONE DYSTROPHY TYPE 1

·  PRA-ROD-CONE DYSTROPHY TYPE 2

·  PRA-ROD-CONE DYSTROPHY TYPE 3

·  PANCREATIC INSUFFICIENCY, EXOCRINE

·  PEMPHIGUS

·  PERSISTENT MULLERIAN DUCT SYNDROME

·  PHOTORECEPTOR DYSPLASIA

·  PLATELET RECEPTOR FOR FACTOR X, DEFICIENCY OF

·  POLYCYSTIC KIDNEY DISEASE

·  PROGRESSIVE RETINAL ATROPHY

·  PROGRESSIVE RETINAL ATROPHY, X-LINKED

·  PYRUVATE KINASE DEFICIENCY OF ERYTHROCYTE

·  RENAL CYSTADENOCARCINOMA AND NODULAR DERMATOFIBROSIS

·  RETINAL DEGENERATION, EARLY

·  RETINAL PIGMENT EPITHELIAL DYSTROPHY

·  ROD-CONE DEGENERATION, PROGRESSIVE

·  SEVERE COMBINED IMMUNODEFICIENCY DISEASE, X-LINKED

·  SEVERE COMBINED IMMUNODEFICIENCY DISEASE, AUTOSOMAL

·  SEX REVERSAL: XX MALE

·  SPINAL MUSCULAR ATROPHY

·  TAIL, SHORT

·  TESTICULAR FEMINIZATION

·  THROMBASTHENIA

·  THROMBOCYTOPAENIA

·  THROMBOXANE RESPONSIVENESS OF PLATELETS

·  TREMOR, X-LINKED

·  VON WILLEBRAND DISEASE

·  VON WILLEBRAND DISEASE I

·  VON WILLEBRAND DISEASE III

·  WILSON DISEASE

·  XANTHINURIA

EMU

·  GANGLIOSIDOSIS

·  MUCOPOLYSACCHARIDOSIS IIIB

FOX

·  CHEDIAK-HIGASHI SYNDROME

·  COAT COLOUR, AGOUTI

·  COAT COLOUR, EXTENSION

GOAT

·  AFIBRINOGENAEMIA

·  GOITRE, FAMILIAL

·  HORNS

·  MANNOSIDOSIS, BETA

·  MUCOPOLYSACCHARIDOSIS IIID

·  PEROMELIA

·  REDUCED CASEIN CONCENTRATION

·  TESTICULAR HYPOPLASIA

GOOSE

·  CREST

GORILLA

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

GUINEA-FOWL

·  FEATHER COLOUR

·  FEATHERING, Z-LINKED

GUINEA-PIG

·  MANNOSIDOSIS, ALPHA

HAMSTER

·  CARDIOMYOPATHY

·  CARDIOMYOPATHY, DILATED

·  CARDIOMYOPATHY, HYPERTROPHIC

·  CIRCADIAN TIMING

·  COAT COLOUR, ALBINISM

·  COAT COLOUR, PINK-EYED DILUTION

·  HAIR LENGTH

·  HIND LIMB PARALYSIS

·  MICROPHTHALMIA

·  WAARDENBURG SYNDROME

HORSE

·  ANTERIOR SEGMENT DYSGENESIS SYNDROME

·  BLOOD GROUP SYSTEM D

·  COAT COLOUR, AGOUTI

·  COAT COLOUR, APPALOOSA

·  COAT COLOUR, BROWN

·  COAT COLOUR, CHAMPAGNE

·  COAT COLOUR, CREAM DILUTION

·  COAT COLOUR, EXTENSION

·  COAT COLOUR, GREY

·  COAT COLOUR, LETHAL DOMINANT ROAN

·  COAT COLOUR, ROAN

·  COAT COLOUR, WHITE, LETHAL, DOMINANT

·  COAT COLOUR, WHITE, LETHAL, RECESSIVE

·  EXOSTOSIS, MULTIPLE

·  GLUCOSE-6-PHOSPHATE DEHYDROGENASE DEFICIENCY

·  GLYCOGEN STORAGE DISEASE IV

·  HAEMOPHILIA A

·  HYPERBILIRUBINAEMIA I

·  MEGACOLON

·  MYOCLONUS

·  PERIODIC PARALYSIS II

·  PROTEIN C DEFICIENCY

·  SEVERE COMBINED IMMUNODEFICIENCY DISEASE, AUTOSOMAL

·  TESTICULAR FEMINIZATION

·  VON WILLEBRAND DISEASE

HUMAN

·  CEROID LIPOFUSCINOSIS

·  CHEDIAK-HIGASHI SYNDROME

LLAMA

·  SEX REVERSAL: XX MALE

LOCUST

·  COAT COLOUR, ALBINISM

MEDAKA

·  COAT COLOUR, ALBINISM

MINK

·  CHEDIAK-HIGASHI SYNDROME

·  COAT COLOUR, BLACK CRYSTAL

·  COAT COLOUR, SILVER-BLUE

·  EHLERS-DANLOS SYNDROME

·  TYROSINE TRANSAMINASE DEFICIENCY

RHESUS

·  ATRICHIA WITH PAPULAR LESIONS in

·  KRABBE DISEASE in

MOUSE

·  CHEDIAK-HIGASHI SYNDROME

DEER

·  SPHEROCYTOSIS in

PIG

·  ARTHROGRYPOSIS

·  ATAXIA, PROGRESSIVE

·  BLOOD GROUP SYSTEM ABO

·  BLOOD GROUP SYSTEM O

·  COAT COLOUR, DOMINANT WHITE

·  COAT COLOUR, EXTENSION

·  DWARFISM

·  GANGLIOSIDOSIS, GM2

·  HAEMOPHILIA A

·  HIND LIMB PARALYSIS

·  HYPERCHOLESTEROLAEMIA

·  HYPOTRICHOSIS, DOMINANT

·  HYPOTRICHOSIS, RECESSIVE

·  LEGLESS

·  LYMPHOSARCOMA

·  MALIGNANT HYPERTHERMIA

·  MEAT QUALITY

·  MEMBRANOPROLIFERATIVE GLOMERULONEPHRITIS TYPE II

·  NEONATAL DIARRHOEA, F4

·  NUCLEOSIDE TRANSPORT DEFECT

·  PORPHYRIA, CONGENITAL ERYTHROPOIETIC

·  PORPHYRIA, UNCLASSIFIED

·  PROGRESSIVE MYOPATHY

·  PROTAMINE-2 DEFICIENCY

·  PSEUDO-VITAMIN D DEFICIENCY RICKETS

·  RENAL CYSTS

·  RESISTANCE TO OEDEMA DISEASE

·  SEX REVERSAL: XX MALE

·  SPERM, SHORT TAIL

·  TREMOR, X-LINKED

·  TREMOR, HIGH-FREQUENCY

·  VON WILLEBRAND DISEASE

·  WOOLLY HAIR

PIGEON

·  ATHEROSCLEROSIS

QUAIL

·  ATYPICAL MITOTIC METAPHASE

·  CHONDRODYSTROPHY

·  CLENCH

·  FEATHER COLOUR, BLACK AT HATCH

·  FEATHER COLOUR, DILUTE DOWN LETHAL

·  FEATHER COLOUR, LIGHT DOWN LETHAL

·  FEATHER COLOUR, ORANGE

·  FEATHER COLOUR, ROUX

·  FEATHER COLOUR, SILVER

·  GLAUCOMA

·  GLYCOGEN STORAGE DISEASE II

·  HEREDITARY MULTIPLE MALFORMATION

·  HYPOTROPHIC AXONOPATHY

·  MICROMELIC SYNDROME

·  MYOTONIC DYSTROPHY

·  OSTEOPETROSIS

·  SHORT BEAK

·  STUMPY LIMB

·  THROAT TUFT

RABBIT

·  ADRENAL HYPERPLASIA, CONGENITAL

·  C3 DEFICIENCY

·  C8 DEFICIENCY

·  COAT COLOUR, ALBINISM

·  CRANIOSYNOSTOSIS

·  EHLERS-DANLOS SYNDROME

·  GLAUCOMA

·  HYPERCHOLESTEROLAEMIA

·  LYMPHOSARCOMA

·  MACROSTOMUS

·  TREMOR, X-LINKED

·  VON WILLEBRAND DISEASE

RAT

·  CHEDIAK-HIGASHI SYNDROME

·  COAT COLOUR, AGOUTI

·  POLYCYSTIC KIDNEY DISEASE

SALAMANDER

·  COAT COLOUR

SHEEP

·  ARGININAEMIA

·  BLOOD GROUP SYSTEM

·  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 I

·  BLOOD GROUP SYSTEM M

·  BLOOD GROUP SYSTEM R

·  BLOOD GROUP SYSTEM X

·  CEROID LIPOFUSCINOSIS, CONGENITAL ONSET, SWEDISH LANDRACE

·  CEROID LIPOFUSCINOSIS, JUVENILE ONSET

·  CHONDRODYSPLASIA

·  COAT COLOUR, AGOUTI

·  COAT COLOUR, ALBINISM

·  COAT COLOUR, EXTENSION

·  DWARFISM, ANCON

·  EHLERS-DANLOS SYNDROME

·  EHLERS-DANLOS SYNDROME, TYPE VII

·  EPIDERMOLYSIS BULLOSA, DYSTROPHIC

·  EPITHELIOGENESIS IMPERFECTA

·  FECUNDITY, BOOROOLA

·  FECUNDITY, CAMBRIDGE

·  FECUNDITY, HANNA

·  FECUNDITY, ICELAND

·  FECUNDITY, INVERDALE

·  FECUNDITY, JAVA

·  FECUNDITY, LACAUNE

·  FECUNDITY, WOODLANDS

·  FRAGILE SITE

·  GANGLIOSIDOSIS, GM1

·