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523 phene records found

[show instead gene records]
OMIA ID Phene Species Scientific Name Species Common Name Gene
OMIA 002134-9913 Abortion due to haplotype AH2Bos tauruscattle RPAP2
OMIA 002033-9913A2 milkBos tauruscattle CSN2
OMIA 001119-9913Abomasum, displacedBos tauruscattle
OMIA 002083-9913Abortion (embryonic lethality), ANXA10-relatedBos tauruscattle ANXA10
OMIA 002042-9913Abortion (embryonic lethality), EXOSC4-relatedBos tauruscattle EXOSC4
OMIA 002043-9913Abortion (embryonic lethality), MED22-relatedBos tauruscattle MED22
OMIA 002039-9913Abortion (embryonic lethality), MYH6-relatedBos tauruscattle MYH6
OMIA 002035-9913Abortion (embryonic lethality), OBFC1-relatedBos tauruscattle OBFC1
OMIA 002037-9913Abortion (embryonic lethality), RABGGTB-relatedBos tauruscattle RABGGTB
OMIA 002038-9913Abortion (embryonic lethality), RNF20-relatedBos tauruscattle RNF20
OMIA 002041-9913Abortion (embryonic lethality), RPIA-relatedBos tauruscattle RPIA
OMIA 002040-9913Abortion (embryonic lethality), SNAPC4-relatedBos tauruscattle SNAPC4
OMIA 002036-9913Abortion (embryonic lethality), TTF1-relatedBos tauruscattle TTF1
OMIA 001565-9913Abortion and stillbirth, MIMT1-relatedBos tauruscattle MIMT1
OMIA 001907-9913Abortion due to haplotype 05-1351 and haplotype 05-1476Bos tauruscattle
OMIA 001906-9913Abortion due to haplotype 05-826Bos tauruscattle
OMIA 001908-9913Abortion due to haplotype 07-126Bos tauruscattle
OMIA 001909-9913Abortion due to haplotype 07-501Bos tauruscattle
OMIA 001910-9913Abortion due to haplotype 11-926, 11-976, 11-1001 and 11,1026Bos tauruscattle
OMIA 001911-9913Abortion due to haplotype 19-151Bos tauruscattle
OMIA 001825-9913Abortion due to haplotype BH1Bos tauruscattle
OMIA 001939-9913Abortion due to haplotype BH2Bos tauruscattle TUBD1
OMIA 001957-9913Abortion due to haplotype FH1Bos tauruscattle
OMIA 001959-9913Abortion due to haplotype FH3Bos tauruscattle
OMIA 001960-9913Abortion due to haplotype FH4Bos tauruscattle SUGT1
OMIA 000001-9913Abortion due to haplotype HH1Bos tauruscattle APAF1
OMIA 001834-9913Abortion due to haplotype HH10Bos tauruscattle
OMIA 001833-9913Abortion due to haplotype HH11Bos tauruscattle
OMIA 001835-9913Abortion due to haplotype HH12Bos tauruscattle
OMIA 001836-9913Abortion due to haplotype HH13Bos tauruscattle
OMIA 001837-9913Abortion due to haplotype HH14Bos tauruscattle
OMIA 001838-9913Abortion due to haplotype HH15Bos tauruscattle
OMIA 001839-9913Abortion due to haplotype HH16Bos tauruscattle
OMIA 001840-9913Abortion due to haplotype HH17Bos tauruscattle
OMIA 001823-9913Abortion due to haplotype HH2Bos tauruscattle
OMIA 001824-9913Abortion due to haplotype HH3Bos tauruscattle SMC2
OMIA 001826-9913Abortion due to haplotype HH4Bos tauruscattle GART
OMIA 001941-9913Abortion due to haplotype HH5Bos tauruscattle TFB1M
OMIA 002149-9913Abortion due to haplotype HH6Bos tauruscattle SDE2
OMIA 001830-9913Abortion due to haplotype HH7Bos tauruscattle CENPU
OMIA 001831-9913Abortion due to haplotype HH8Bos tauruscattle
OMIA 001832-9913Abortion due to haplotype HH9Bos tauruscattle
OMIA 001697-9913Abortion due to haplotype JH1Bos tauruscattle CWC15
OMIA 001942-9913Abortion due to haplotype JH2Bos tauruscattle
OMIA 001827-9913Abortion due to haplotype MH1Bos tauruscattle PFAS
OMIA 001849-9913Abortion due to haplotype MH10Bos tauruscattle
OMIA 001850-9913Abortion due to haplotype MH11Bos tauruscattle
OMIA 001828-9913Abortion due to haplotype MH2Bos tauruscattle SLC37A2
OMIA 001842-9913Abortion due to haplotype MH3Bos tauruscattle
OMIA 001843-9913Abortion due to haplotype MH4Bos tauruscattle
OMIA 001844-9913Abortion due to haplotype MH5Bos tauruscattle
OMIA 001845-9913Abortion due to haplotype MH6Bos tauruscattle
OMIA 001846-9913Abortion due to haplotype MH7Bos tauruscattle
OMIA 001847-9913Abortion due to haplotype MH8Bos tauruscattle
OMIA 001848-9913Abortion due to haplotype MH9Bos tauruscattle
OMIA 001851-9913Abortion due to haplotype NH1Bos tauruscattle
OMIA 001852-9913Abortion due to haplotype NH2Bos tauruscattle
OMIA 001853-9913Abortion due to haplotype NH3Bos tauruscattle
OMIA 001854-9913Abortion due to haplotype NH4Bos tauruscattle
OMIA 001829-9913Abortion due to haplotype NH5Bos tauruscattle
OMIA 001855-9913Abortion due to haplotype NH6Bos tauruscattle
OMIA 001901-9913Abortion, RNASEH2B-relatedBos tauruscattle RNASEH2B
OMIA 000002-9913AbrachiaBos tauruscattle
OMIA 001926-9913Achondrogenesis, type IIBos tauruscattle COL2A1
OMIA 000004-9913AchondroplasiaBos tauruscattle
OMIA 000005-9913Achondroplasia foetalisBos tauruscattle
OMIA 000593-9913Acrodermatitis enteropathicaBos tauruscattle SLC39A4
OMIA 000010-9913Acroteriasis congenitaBos tauruscattle
OMIA 000012-9913AdactylyBos tauruscattle
OMIA 000014-9913Adenohypophyseal aplasiaBos tauruscattle
OMIA 000021-9913Agenesis of corpus callosumBos tauruscattle
OMIA 000022-9913AgnathiaBos tauruscattle
OMIA 000027-9913Allergic rhinitisBos tauruscattle
OMIA 001702-9913Alopecia areataBos tauruscattle
OMIA 000030-9913Alopecia, genericBos tauruscattle
OMIA 000824-9913Alopecia, progressiveBos tauruscattle
OMIA 000036-9913AmputatedBos tauruscattle
OMIA 000038-9913Amyloidosis, AABos tauruscattle
OMIA 000040-9913Amyloidosis, renalBos tauruscattle
OMIA 000991-9913Androgen insensitivity syndrome (AIS)Bos tauruscattle
OMIA 000044-9913AnencephalyBos tauruscattle
OMIA 000543-9913Anhidrotic ectodermal dysplasia, EDA-relatedBos tauruscattle EDA
OMIA 002128-9913Anhidrotic ectodermal dysplasia, EDAR-relatedBos tauruscattle EDAR
OMIA 000047-9913Ankylosis, generalisedBos tauruscattle
OMIA 001556-9913Ankylosis, jawBos tauruscattle
OMIA 000049-9913AnophthalmosBos tauruscattle
OMIA 000050-9913Anophthalmos microphthalmosBos tauruscattle
OMIA 001411-9913AnotiaBos tauruscattle
OMIA 000056-9913Aplasia segmentalis ductus wolffiiBos tauruscattle
OMIA 000058-9913AprosopiaBos tauruscattle
OMIA 001541-9913Arachnomelia, BTA23Bos tauruscattle MOCS1
OMIA 000059-9913Arachnomelia, BTA5Bos tauruscattle SUOX
OMIA 000061-9913Arnold-Chiari malformationBos tauruscattle
OMIA 000070-9913Arthrogryposis and palatoschisis syndromeBos tauruscattle
OMIA 002135-9913Arthrogryposis multiplex congenita, AGRN-relatedBos tauruscattle AGRN
OMIA 002022-9913Arthrogryposis multiplex congenita, CHRNB1-relatedBos tauruscattle CHRNB1
OMIA 001465-9913Arthrogryposis multiplex congenita, genericBos tauruscattle
OMIA 001978-9913Arthrogryposis, distal, type 1BBos tauruscattle MYBPC1
OMIA 000069-9913Arthrogryposis, genericBos tauruscattle
OMIA 001953-9913Arthrogryposis, lethal syndromeBos tauruscattle PIGH
OMIA 001169-9913AscitesBos tauruscattle
OMIA 002091-9913Ataxia, cerebellar, genericBos tauruscattle
OMIA 000077-9913Ataxia, genericBos tauruscattle
OMIA 001091-9913Ataxia, progressiveBos tauruscattle
OMIA 000083-9913Atresia aniBos tauruscattle
OMIA 000085-9913Atresia coliBos tauruscattle
OMIA 000086-9913Atresia ileiBos tauruscattle
OMIA 000087-9913Atresia intestinalBos tauruscattle
OMIA 000089-9913Atrial septal defectBos tauruscattle
OMIA 000091-9913Atrophic rhinitisBos tauruscattle
OMIA 001106-9913AxonopathyBos tauruscattle MFN2
OMIA 001437-9913Beta-lactoglobulin, aberrant low expressionBos tauruscattle PAEP
OMIA 000110-9913Black hair follicle dysplasiaBos tauruscattle
OMIA 000112-9913Bleeding diathesisBos tauruscattle
OMIA 000113-9913Bleeding disorderBos tauruscattle
OMIA 000117-9913Blood group system ABos tauruscattle
OMIA 000120-9913Blood group system BBos tauruscattle
OMIA 000121-9913Blood group system CBos tauruscattle
OMIA 000124-9913Blood group system FBos tauruscattle
OMIA 000130-9913Blood group system JBos tauruscattle
OMIA 000132-9913Blood group system LBos tauruscattle
OMIA 000133-9913Blood group system MBos tauruscattle
OMIA 001629-9913Blood group system N'Bos tauruscattle
OMIA 001630-9913Blood group system R'Bos tauruscattle
OMIA 000139-9913Blood group system SBos tauruscattle
OMIA 001631-9913Blood group system T'Bos tauruscattle
OMIA 001632-9913Blood group system ZBos tauruscattle
OMIA 000116-9913Blood group systems, genericBos tauruscattle
OMIA 000147-9913BrachygnathiaBos tauruscattle
OMIA 000149-9913Brachygnathia superiorBos tauruscattle
OMIA 000150-9913Brachygnathia superior and degenerative joint diseaseBos tauruscattle
OMIA 000151-9913BrachyspinaBos tauruscattle FANCI
OMIA 001502-9913Caprine-like Generalized Hypoplasia SyndromeBos tauruscattle CEP250
OMIA 000159-9913Cardiac anomalyBos tauruscattle
OMIA 000160-9913CardiomyopathyBos tauruscattle
OMIA 000161-9913Cardiomyopathy and woolly haircoat syndromeBos tauruscattle PPP1R13L
OMIA 000162-9913Cardiomyopathy, dilatedBos tauruscattle OPA3
OMIA 000515-9913Cardiomyopathy, hypertrophicBos tauruscattle
OMIA 000168-9913Cataract, genericBos tauruscattle
OMIA 002111-9913Cataract, recessive, CPAMD8-relatedBos tauruscattle CPAMD8
OMIA 001936-9913Cataract, recessive, NID1-relatedBos tauruscattle NID1
OMIA 000175-9913Cerebellar abiotrophyBos tauruscattle
OMIA 000177-9913Cerebellar cortical atrophyBos tauruscattle
OMIA 000178-9913Cerebellar diseaseBos tauruscattle
OMIA 000179-9913Cerebellar hypoplasiaBos tauruscattle
OMIA 000185-9913Chediak-Higashi syndromeBos tauruscattle LYST
OMIA 000187-9913ChondrodysplasiaBos tauruscattle EVC2
OMIA 000189-9913ChondrodystrophyBos tauruscattle
OMIA 000194-9913CitrullinaemiaBos tauruscattle ASS1
OMIA 000195-9913Claw defectsBos tauruscattle
OMIA 001585-9913Cleft lip and jaw, right-sidedBos tauruscattle
OMIA 001714-9913Cleft lip and palateBos tauruscattle
OMIA 000197-9913Cleft palateBos tauruscattle
OMIA 000201-9913Coat colour, agoutiBos tauruscattle ASIP
OMIA 000202-9913Coat colour, albinismBos tauruscattle TYR
OMIA 000204-9913Coat colour, albinism, incompleteBos tauruscattle
OMIA 001821-9913Coat colour, albinism, oculocutaneous type IVBos tauruscattle SLC45A2
OMIA 001249-9913Coat colour, brownBos tauruscattle TYRP1
OMIA 001576-9913Coat colour, colour-sidedBos tauruscattle KIT
OMIA 000031-9913Coat colour, diluteBos tauruscattle MLPH
OMIA 001545-9913Coat colour, dilutionBos tauruscattle PMEL
OMIA 001529-9913Coat colour, dominant redBos tauruscattle COPA
OMIA 000209-9913Coat colour, dominant whiteBos tauruscattle KIT
OMIA 001199-9913Coat colour, extensionBos tauruscattle MC1R
OMIA 001216-9913Coat colour, roanBos tauruscattle KITLG
OMIA 001320-9913Coat colour, spottedBos tauruscattle
OMIA 001469-9913Coat colour, white beltBos tauruscattle TWIST2
OMIA 000214-9913Coat colour, white spottingBos tauruscattle MITF
OMIA 000200-9913Coat colours, genericBos tauruscattle
OMIA 000219-9913ColobomaBos tauruscattle
OMIA 001340-9913Complex vertebral malformationBos tauruscattle SLC35A3
OMIA 001814-9913Congenital chondrodystrophy of unknown origin Bos tauruscattle
OMIA 000313-9913Congenital dyserythropoietic anaemia with dyskeratosis and progressive alopeciaBos tauruscattle
OMIA 001689-9913Congenital hydranencephaly and cerebellar hypoplasiaBos tauruscattle
OMIA 001450-9913Congenital muscular dystonia 1Bos tauruscattle ATP2A1
OMIA 001451-9913Congenital muscular dystonia 2Bos tauruscattle LOC528050
OMIA 001511-9913Contractural arachnodactyly (Fawn calf syndrome)Bos tauruscattle ADAMTSL3
OMIA 001270-9913Convulsions and ataxia, familialBos tauruscattle
OMIA 002104-9913Corkscrew clawBos tauruscattle
OMIA 001118-9913Corkscrew penisBos tauruscattle
OMIA 000231-9913Corneal opacityBos tauruscattle
OMIA 000235-9913Cranial duplicationBos tauruscattle
OMIA 000237-9913CranioschisisBos tauruscattle
OMIA 000243-9913CryptorchidismBos tauruscattle
OMIA 000245-9913Curly coatBos tauruscattle
OMIA 000246-9913Curly hair, karakul-typeBos tauruscattle KRT27
OMIA 000249-9913CyclopiaBos tauruscattle
OMIA 000254-9913Cystic ovaryBos tauruscattle
OMIA 000260-9913Debility, congenitalBos tauruscattle
OMIA 000261-9913Defective keratogenesis of hooves and mouthBos tauruscattle
OMIA 000262-9913Deficiency of uridine monophosphate synthaseBos tauruscattle UMPS
OMIA 001931-9913Depigmentation associated with microphthalmiaBos tauruscattle MITF
OMIA 000272-9913Dermoid sinusBos tauruscattle
OMIA 000274-9913Dermoid, ocular, congenitalBos tauruscattle
OMIA 002103-9913Developmental duplicationsBos tauruscattle NHLRC2
OMIA 000279-9913Diabetes mellitusBos tauruscattle
OMIA 000283-9913Diabetes mellitus, type IBos tauruscattle
OMIA 001410-9913DiphallusBos tauruscattle
OMIA 000290-9913DiprosopusBos tauruscattle
OMIA 001841-9913DistichiasisBos tauruscattle
OMIA 000291-9913DoddlerBos tauruscattle
OMIA 001680-9913Dominant white with bilateral deafnessBos tauruscattle MITF
OMIA 000293-9913Double cervixBos tauruscattle
OMIA 000295-9913Duck-leggedBos tauruscattle
OMIA 000299-9913DwarfismBos tauruscattle
OMIA 001271-9913Dwarfism, ACAN-relatedBos tauruscattle ACAN
OMIA 001485-9913Dwarfism, AngusBos tauruscattle PRKG2
OMIA 001659-9913Dwarfism, dominantBos tauruscattle
OMIA 001985-9913Dwarfism, FleckviehBos tauruscattle GON4L
OMIA 001473-9913Dwarfism, growth-hormone deficiencyBos tauruscattle GH1
OMIA 001294-9913Dwarfism, growth-hormone-receptor deficiencyBos tauruscattle
OMIA 001323-9913Dwarfism, LaronBos tauruscattle
OMIA 000308-9913Dwarfism, proportionateBos tauruscattle
OMIA 001686-9913Dwarfism, proportionate, with inflammatory lesionsBos tauruscattle RNF11
OMIA 000310-9913Dwarfism, snorterBos tauruscattle
OMIA 000311-9913Dwarfism, stumpyBos tauruscattle
OMIA 000317-9913Ears, cropBos tauruscattle HMX1
OMIA 000318-9913Ears, doubleBos tauruscattle
OMIA 000324-9913EctrodactylyBos tauruscattle
OMIA 001126-9913EctromeliaBos tauruscattle
OMIA 001716-9913Ehlers-Danlos syndrome, Holstein variantBos tauruscattle EPYC
OMIA 000328-9913Ehlers-Danlos syndrome, type VII (Dermatosparaxis)Bos tauruscattle ADAMTS2
OMIA 001488-9913Encephalomyelopathy, multifocal symmetrical necrotizing, AngusBos tauruscattle
OMIA 001489-9913Encephalomyelopathy, multifocal symmetrical necrotizing, LimousinBos tauruscattle
OMIA 001490-9913Encephalomyelopathy, multifocal symmetrical necrotizing, SimmentalBos tauruscattle
OMIA 001803-9913Endocardial fibroelastosisBos tauruscattle
OMIA 000337-9913EntropionBos tauruscattle
OMIA 000338-9913Epidermal dysplasiaBos tauruscattle
OMIA 000339-9913EpidermolysisBos tauruscattle
OMIA 000340-9913Epidermolysis bullosaBos tauruscattle
OMIA 000341-9913Epidermolysis bullosa, dystrophicBos tauruscattle COL7A1
OMIA 000342-9913Epidermolysis bullosa, junctionalisBos tauruscattle
OMIA 001948-9913Epidermolysis bullosa, junctionalis, ITGB4-relatedBos tauruscattle ITGB4
OMIA 001677-9913Epidermolysis bullosa, junctionalis, LAMA3-relatedBos tauruscattle LAMA3
OMIA 001678-9913Epidermolysis bullosa, junctionalis, LAMC2-relatedBos tauruscattle LAMC2
OMIA 002082-9913Epidermolysis bullosa, simplexBos tauruscattle
OMIA 002081-9913Epidermolysis bullosa, simplex, KRT5-relatedBos tauruscattle KRT5
OMIA 000343-9913Epididymal aplasiaBos tauruscattle
OMIA 000344-9913EpilepsyBos tauruscattle Gene not yet published
OMIA 001239-9913EpiphoraBos tauruscattle
OMIA 000346-9913EpistaxisBos tauruscattle
OMIA 000348-9913Epitheliogenesis imperfectaBos tauruscattle
OMIA 000353-9913Exophthalmos with strabismusBos tauruscattle
OMIA 000355-9913Extra ear lobesBos tauruscattle
OMIA 000358-9913Eye defectsBos tauruscattle
OMIA 000360-9913Facial digital syndromeBos tauruscattle
OMIA 002090-9913Facial dysplasia syndromeBos tauruscattle FGFR2
OMIA 001276-9913Facial eczemaBos tauruscattle
OMIA 000363-9913Factor XI deficiencyBos tauruscattle F11
OMIA 001818-9913Factor XIII deficiencyBos tauruscattle
OMIA 000366-9913Fanconi syndromeBos tauruscattle SLC2A2
OMIA 001943-9913FecundityBos tauruscattle
OMIA 001442-9913Forelimb-girdle muscular anomalyBos tauruscattle GFRA1
OMIA 000391-9913Fragile XBos tauruscattle
OMIA 000393-9913FreemartinBos tauruscattle
OMIA 000401-9913GangliosidosisBos tauruscattle
OMIA 000402-9913Gangliosidosis, GM1Bos tauruscattle
OMIA 000406-9913Genital hypoplasiaBos tauruscattle
OMIA 000410-9913Glandular aplasiaBos tauruscattle
OMIA 000419-9913Glycogen storage disease IIBos tauruscattle GAA
OMIA 001139-9913Glycogen storage disease VBos tauruscattle PYGM
OMIA 000424-9913Goitre, familialBos tauruscattle TG
OMIA 000426-9913Gonadal hypoplasiaBos tauruscattle KIT
OMIA 001958-9913Growth retardation due to haplotype FH2Bos tauruscattle
OMIA 001813-9913HaemangiosarcomaBos tauruscattle
OMIA 000428-9913HaemochromatosisBos tauruscattle
OMIA 000430-9913Haemolytic anaemiaBos tauruscattle
OMIA 000435-9913Haemolytic uremic syndromeBos tauruscattle
OMIA 000437-9913Haemophilia ABos tauruscattle F8
OMIA 000439-9913Hair, longBos tauruscattle
OMIA 000441-9913HairyBos tauruscattle PRL
OMIA 000444-9913HarelipBos tauruscattle
OMIA 000446-9913Heart defect, congenitalBos tauruscattle
OMIA 001667-9913Heat toleranceBos tauruscattle
OMIA 000726-9913HemeralopiaBos tauruscattle
OMIA 001191-9913HemivertebraeBos tauruscattle
OMIA 000454-9913Hepatic fibrosis, idiopathicBos tauruscattle
OMIA 000457-9913Hernia, brainBos tauruscattle
OMIA 000462-9913Hernia, inguinalBos tauruscattle
OMIA 000464-9913Hernia, scrotalBos tauruscattle
OMIA 000465-9913Hernia, umbilicalBos tauruscattle
OMIA 000466-9913Hernia, ventralBos tauruscattle
OMIA 000468-9913Heterochromia irides/iridisBos tauruscattle
OMIA 000470-9913High lysozyme activityBos tauruscattle
OMIA 000473-9913Hip dysplasiaBos tauruscattle
OMIA 000620-9913Histiocytosis, malignantBos tauruscattle
OMIA 000474-9913HistocytosisBos tauruscattle
OMIA 000475-9913Hocks, straightBos tauruscattle
OMIA 001965-9913Holstein cholesterol deficiency Bos tauruscattle APOB
OMIA 001197-9913Horner syndromeBos tauruscattle
OMIA 000484-9913Horse rumpBos tauruscattle
OMIA 002053-9913HydrallantoisBos tauruscattle SLC12A1
OMIA 000486-9913HydranencephalyBos tauruscattle
OMIA 000487-9913HydrocephalusBos tauruscattle Gene not yet published
OMIA 000489-9913Hydrocephalus, internalBos tauruscattle
OMIA 000493-9913Hydrops foetalisBos tauruscattle
OMIA 001107-9913Hymen, imperforateBos tauruscattle
OMIA 000495-9913Hyperbilirubinaemia, unclassifiedBos tauruscattle
OMIA 001412-9913Hyperextension of fetlock jointsBos tauruscattle
OMIA 001231-9913HyperhidrosisBos tauruscattle
OMIA 000506-9913HypermetriaBos tauruscattle
OMIA 002052-9913HyperphosphatemiaBos tauruscattle
OMIA 000513-9913HypertrichosisBos tauruscattle
OMIA 002048-9913Hypocalcemia, subclinicalBos tauruscattle
OMIA 002051-9913HypokalemiaBos tauruscattle
OMIA 002050-9913Hypomagnesemia, subclinicalBos tauruscattle
OMIA 000527-9913Hypomyelinogenesis, congenitalBos tauruscattle KIF1C
OMIA 001184-9913HypophosphataemiaBos tauruscattle
OMIA 000530-9913Hypoplasia of sex organsBos tauruscattle
OMIA 001187-9913HypospadiasBos tauruscattle
OMIA 000540-9913HypotrichosisBos tauruscattle HEPHL1
OMIA 001544-9913Hypotrichosis with coat-colour dilution (rat-tail syndrome)Bos tauruscattle
OMIA 002114-9913Hypotrichosis, KRT71-relatedBos tauruscattle KRT71
OMIA 000541-9913Hypotrichosis, semiBos tauruscattle
OMIA 000542-9913Hypotrichosis, streakedBos tauruscattle TSR2
OMIA 000547-9913Ichthyosis congenitaBos tauruscattle ABCA12
OMIA 000555-9913Immunoglobulin G2 deficiencyBos tauruscattle
OMIA 000558-9913Imperforate anusBos tauruscattle
OMIA 000560-9913Impotentia cocundiBos tauruscattle
OMIA 000562-9913InfertilityBos tauruscattle
OMIA 000563-9913Interdigital tissue pachydermiaBos tauruscattle
OMIA 000564-9913IntersexBos tauruscattle
OMIA 002047-9913Intersex: XX, SRY-positiveBos tauruscattle
OMIA 001227-9913IntussusceptionBos tauruscattle
OMIA 002102-9913Iridal hypopigmentation, bilateralBos tauruscattle
OMIA 000570-9913Joint laxity and dwarfism, congenitalBos tauruscattle
OMIA 001125-9913KetosisBos tauruscattle
OMIA 000576-9913Knobbed acrosomeBos tauruscattle
OMIA 001693-9913Lacrimal fistulaBos tauruscattle
OMIA 000579-9913LamenessBos tauruscattle
OMIA 001225-9913LaminitisBos tauruscattle
OMIA 001206-9913Laryngeal paralysisBos tauruscattle
OMIA 000584-9913Leg defectsBos tauruscattle
OMIA 000585-9913Leg weaknessBos tauruscattle
OMIA 001404-9913Leptin concentrationBos tauruscattle
OMIA 000590-9913Lethal geneBos tauruscattle
OMIA 001722-9913Lethal multi-organ developmental dysplasiaBos tauruscattle KDM2B
OMIA 000595-9913Leukocyte adhesion deficiency, type IBos tauruscattle ITGB2
OMIA 000599-9913Limb deformity, congenitalBos tauruscattle
OMIA 000601-9913Limber legsBos tauruscattle
OMIA 000603-9913Limbs, curvedBos tauruscattle
OMIA 000605-9913Lipidosis, hepaticBos tauruscattle
OMIA 001407-9913Lipofuscinosis, renalBos tauruscattle
OMIA 000606-9913Lipomatosis, multipleBos tauruscattle
OMIA 001557-9913Ljutikow's lethalBos tauruscattle
OMIA 000613-9913LymphoedemaBos tauruscattle
OMIA 000616-9913Lysosomal storage diseaseBos tauruscattle
OMIA 001902-9913Male subfertilityBos tauruscattle TMEM95
OMIA 000621-9913Malignant hyperthermiaBos tauruscattle
OMIA 000625-9913Mannosidosis, alphaBos tauruscattle MAN2B1
OMIA 000626-9913Mannosidosis, betaBos tauruscattle MANBA
OMIA 000627-9913Maple syrup urine diseaseBos tauruscattle BCKDHA
OMIA 000628-9913Marfan syndromeBos tauruscattle FBN1
OMIA 000629-9913MegacolonBos tauruscattle
OMIA 000631-9913MegaoesophagusBos tauruscattle
OMIA 001860-9913Methane emissionsBos tauruscattle
OMIA 000644-9913MicrencephalyBos tauruscattle
OMIA 000646-9913MicrognathiaBos tauruscattle
OMIA 000647-9913MicrohydranencephalusBos tauruscattle
OMIA 001558-9913Micromelia, achondroplasticBos tauruscattle
OMIA 000649-9913MicrophthalmiaBos tauruscattle
OMIA 000656-9913Molars, impactedBos tauruscattle
OMIA 000664-9913Mucopolysaccharidosis IBos tauruscattle
OMIA 001342-9913Mucopolysaccharidosis IIIBBos tauruscattle NAGLU
OMIA 000733-9913Multiple ocular defectsBos tauruscattle WFDC1
OMIA 000673-9913Mummified foetusBos tauruscattle
OMIA 000674-9913Muscle contractureBos tauruscattle
OMIA 000675-9913Muscle contracture and chondrodysplasiaBos tauruscattle
OMIA 000683-9913Muscular hypertrophy (double muscling)Bos tauruscattle MSTN
OMIA 000685-9913Myasthenic syndrome, congenital, CHRNE-relatedBos tauruscattle CHRNE
OMIA 000827-9913Myeloencephalopathy, progressive degenerative (Weaver syndrome)Bos tauruscattle PNPLA8
OMIA 000689-9913MyoclonusBos tauruscattle GLRA1
OMIA 000690-9913Myoclonus epilepsy of LaforaBos tauruscattle
OMIA 001319-9913Myopathy of the diaphragmatic musclesBos tauruscattle HSPA1A
OMIA 000697-9913Myositis ossificansBos tauruscattle
OMIA 000698-9913MyotoniaBos tauruscattle
OMIA 001097-9913Necrotising encephalopathy, subacute, of LeighBos tauruscattle
OMIA 002125-9913NeurocristopathyBos tauruscattle CHD7
OMIA 000716-9913NeurofibromatosisBos tauruscattle
OMIA 001351-9913Neuromuscular disease, degenerativeBos tauruscattle
OMIA 001482-9913Neuronal ceroid lipofuscinosis, 5Bos tauruscattle CLN5
OMIA 000181-9913Neuronal Ceroid Lipofuscinosis, genericBos tauruscattle
OMIA 001795-9913Niemann-Pick disease, type ABos tauruscattle
OMIA 000728-9913Nipples, depressedBos tauruscattle
OMIA 000729-9913Nipples, invertedBos tauruscattle
OMIA 000735-9913Ocular squamous cell carcinomaBos tauruscattle
OMIA 002101-9913Oculocutaneous hypopigmentationBos tauruscattle Gene not yet published
OMIA 000741-9913OmphaloceleBos tauruscattle
OMIA 000747-9913OsteoarthritisBos tauruscattle
OMIA 000750-9913OsteochondrosisBos tauruscattle
OMIA 000753-9913OsteodystrophyBos tauruscattle
OMIA 000754-9913Osteogenesis imperfecta, genericBos tauruscattle
OMIA 002127-9913Osteogenesis imperfecta, type II, COL1A1-relatedBos tauruscattle COL1A1
OMIA 000755-9913OsteopetrosisBos tauruscattle SLC4A2
OMIA 001887-9913Osteopetrosis with gingival hamartomasBos tauruscattle CLCN7
OMIA 001277-9913Otitis interna, susceptibility toBos tauruscattle
OMIA 001266-9913Otitis media, susceptibility toBos tauruscattle
OMIA 001127-9913OtocephalyBos tauruscattle
OMIA 000759-9913Ovarian aplasiaBos tauruscattle
OMIA 000761-9913Ovarian hypoplasiaBos tauruscattle
OMIA 001230-9913Ovotesticular DSD (Disorder of Sexual Development)Bos tauruscattle SRY
OMIA 001539-9913Pancytopenia, neonatalBos tauruscattle
OMIA 001147-9913Papillomatosis, cutaneousBos tauruscattle
OMIA 002154-9913Paratuberculosis, resistance toBos tauruscattle
OMIA 000775-9913Pasterns, bowedBos tauruscattle
OMIA 000776-9913Pasterns, flexedBos tauruscattle
OMIA 000778-9913Patellar luxationBos tauruscattle
OMIA 000779-9913Patent ductus arteriosusBos tauruscattle
OMIA 001188-9913PemphigusBos tauruscattle
OMIA 001817-9913Perinatal weak calf syndromeBos tauruscattle IARS
OMIA 001453-9913Periodic spasticity, inheritedBos tauruscattle
OMIA 000789-9913Perosomus elumbisBos tauruscattle
OMIA 000792-9913Persistent frenulum praeputiiBos tauruscattle
OMIA 000795-9913Persistent truncus arteriosusBos tauruscattle
OMIA 001218-9913Persistent truncus arteriosus with ventricular septal defect and patent foramen ovaleBos tauruscattle
OMIA 000798-9913Phalanges, reducedBos tauruscattle
OMIA 000803-9913Platelet function defectBos tauruscattle
OMIA 001736-9913Polled and multisystemic syndromeBos tauruscattle ZEB2
OMIA 000483-9913Polled/HornsBos tauruscattle POLL
OMIA 000809-9913PolycythemiaBos tauruscattle
OMIA 000810-9913PolydactylyBos tauruscattle
OMIA 001226-9913PolymeliaBos tauruscattle
OMIA 001100-9913PolymicrogyriaBos tauruscattle
OMIA 001175-9913Porphyria, congenital erythropoieticBos tauruscattle
OMIA 000817-9913Portosystemic shuntBos tauruscattle
OMIA 001265-9913Preputial prolapse/eversionBos tauruscattle
OMIA 000823-9913PrognathismBos tauruscattle
OMIA 000832-9913Progressive spinal myelopathyBos tauruscattle
OMIA 000833-9913Prolonged gestationBos tauruscattle
OMIA 000834-9913Protamine-2 deficiencyBos tauruscattle
OMIA 000836-9913ProtoporphyriaBos tauruscattle FECH
OMIA 001464-9913Pseudomyotonia, congenitalBos tauruscattle ATP2A1
OMIA 001934-9913Ptosis, intellectual disability, retarded growth and mortality (PIRM) syndromeBos tauruscattle UBE3B
OMIA 000840-9913Pulmonary adenomatosisBos tauruscattle
OMIA 000841-9913Pulmonary hypertensionBos tauruscattle
OMIA 001562-9913Pulmonary hypoplasia with anasarcaBos tauruscattle Gene not yet published
OMIA 001691-9913Recombination rateBos tauruscattle
OMIA 000850-9913Rectovaginal constrictionBos tauruscattle
OMIA 001135-9913Renal dysplasiaBos tauruscattle CLDN16
OMIA 001533-9913Resistance to infectious bovine keratoconjunctivitis,Bos tauruscattle
OMIA 001744-9913Resistance to mastitisBos tauruscattle
OMIA 001905-9913Resistance/susceptibility to Johne's diseaseBos tauruscattle
OMIA 002073-9913Resistance/susceptibility to Mannheimia haemolytica leukotoxinBos tauruscattle ITGB2
OMIA 000866-9913Retinal degenerationBos tauruscattle
OMIA 001663-9913Retinal dysplasia and internal hydrocephalusBos tauruscattle
OMIA 001413-9913Retinitis pigmentosaBos tauruscattle
OMIA 002029-9913Retinitis pigmentosa 1Bos tauruscattle RP1
OMIA 001921-9913Rhabdomyosarcoma, embryonalBos tauruscattle
OMIA 000890-9913Schistosomus reflexusBos tauruscattle
OMIA 001963-9913SchwannomatosisBos tauruscattle
OMIA 000894-9913ScursBos tauruscattle
OMIA 001593-9913Scurs, type 2Bos tauruscattle TWIST1
OMIA 000896-9913Seminal defectBos tauruscattle
OMIA 000898-9913Serum cholesterol levelBos tauruscattle
OMIA 000908-9913Sheep's headBos tauruscattle
OMIA 000911-9913Short spineBos tauruscattle
OMIA 001102-9913Situs inversusBos tauruscattle
OMIA 000917-9913Skeletal deformityBos tauruscattle
OMIA 000919-9913Skin defectBos tauruscattle
OMIA 001372-9913Slick hairBos tauruscattle PRLR
OMIA 000922-9913Smooth tongueBos tauruscattle
OMIA 000926-9913Spastic lamenessBos tauruscattle
OMIA 000927-9913Spastic lethalBos tauruscattle
OMIA 000928-9913Spastic paresisBos tauruscattle
OMIA 000929-9913Spastic syndromeBos tauruscattle
OMIA 000930-9913Sperm defectBos tauruscattle
OMIA 000932-9913Sperm, dag defect ofBos tauruscattle
OMIA 001662-9913Sperm, decapitatedBos tauruscattle
OMIA 001334-9913Sperm, short tailBos tauruscattle ARMC3
OMIA 001228-9913SpherocytosisBos tauruscattle SLC4A1
OMIA 000933-9913Spina bifidaBos tauruscattle
OMIA 000935-9913Spina bifida with myelomeningoceleBos tauruscattle
OMIA 001247-9913Spinal dysmyelinationBos tauruscattle SPAST
OMIA 000938-9913Spinal dysraphismBos tauruscattle
OMIA 000939-9913Spinal muscular atrophyBos tauruscattle KDSR
OMIA 000944-9913Spongiform encephalopathyBos tauruscattle PRNP
OMIA 001156-9913Spongiform myelopathyBos tauruscattle
OMIA 000947-9913Stenosis, spinalBos tauruscattle
OMIA 001991-9913StillbirthBos tauruscattle
OMIA 000950-9913StringhaltBos tauruscattle
OMIA 000963-9913Syndactyly (mule foot)Bos tauruscattle LRP4
OMIA 002150-9913Syndrome des veaux tourneurs (Turning calves syndrome)Bos tauruscattle SLC25A46
OMIA 000965-9913SyringomyeliaBos tauruscattle
OMIA 001452-9913Tail, crookedBos tauruscattle MRC2
OMIA 000973-9913Tail, kinkyBos tauruscattle
OMIA 000975-9913Tail, shortBos tauruscattle
OMIA 001510-9913Tail, wryBos tauruscattle
OMIA 000977-9913TaillessnessBos tauruscattle
OMIA 000984-9913Teat injuryBos tauruscattle
OMIA 000985-9913Teat/nipple numberBos tauruscattle
OMIA 000986-9913Teats, bottleBos tauruscattle
OMIA 000987-9913Teats, fusedBos tauruscattle
OMIA 000990-9913Tendons, contracted, congenitalBos tauruscattle
OMIA 000992-9913Testicular hypoplasiaBos tauruscattle
OMIA 000994-9913Tetralogy of fallotBos tauruscattle
OMIA 000997-9913Thoracic limb, angular deformity ofBos tauruscattle
OMIA 001001-9913ThrombocytopeniaBos tauruscattle
OMIA 001003-9913ThrombopathiaBos tauruscattle RASGRP2
OMIA 001009-9913Tibial hemimeliaBos tauruscattle ALX4
OMIA 001491-9913Tomaculous neuropathyBos tauruscattle
OMIA 001012-9913Tongue-waggingBos tauruscattle
OMIA 002109-9913Tricho-dento-osseous-like syndromeBos tauruscattle DLX3
OMIA 001360-9913Trimethylaminuria (fishy taint)Bos tauruscattle FMO3
OMIA 001856-9913Tuberculosis, susceptibility/resistance toBos tauruscattle
OMIA 001022-9913TwinningBos tauruscattle
OMIA 001023-9913Twinning, conjoinedBos tauruscattle
OMIA 001026-9913Udder abnormalityBos tauruscattle
OMIA 001033-9913UrolithiasisBos tauruscattle
OMIA 001039-9913Various disordersBos tauruscattle
OMIA 001041-9913Ventricular septal defectBos tauruscattle
OMIA 001043-9913Ventricular septal defect with atrioventricular valvular anomalyBos tauruscattle
OMIA 001951-9913Vertebral and spinal dysplasiaBos tauruscattle T
OMIA 001048-9913Vertical fibre hide defectBos tauruscattle
OMIA 001055-9913VitiligoBos tauruscattle
OMIA 001056-9913Von Willebrand disease, genericBos tauruscattle
OMIA 001060-9913Warts between hoovesBos tauruscattle
OMIA 001142-9913Wilms tumourBos tauruscattle
OMIA 001071-9913Wilson diseaseBos tauruscattle
OMIA 001194-9913Wolff-Parkinson-White syndromeBos tauruscattle
OMIA 001819-9913Xanthinuria, type IIBos tauruscattle MOCOS
OMIA 001769-9913Y anomaly in low reproductive females Bos tauruscattle
OMIA 001079-9913Yellow fatBos tauruscattle BCO2
OMIA 001935-9913Zinc deficiency-like syndromeBos tauruscattle PLD4