VH Aladdin - FRA 2912558080

Production & Efficiency

Trait Index 80 100 120
Production 121
Milk kg 107
Fat, kg 125
Fat, % 114
Protein kg 113
Protein % 107
Persistency 96
Growth 100
Daily carcass gain 100
Carcass conformation score 100
Saved feed 103
Maintenance efficiency 110

NAV proof run date: 02-12-2025 Reliability 90 % Number of daughters: 6

Expected Progeny Difference

Trait Index Bull effect Average
Milk lbs, 305 days 107 506.18 25,646.37
Fat lbs, 305 days 125 68.78 1,051.60
Fat %, 305 days 114 0.22 4.2
Protein lbs, 305 days 113 28.66 901.69
Protein %, 305 days 107 0.05 3.5

NAV proof run date: 02-12-2025 Reliability 90 % Number of daughters: 6

Health & Reproduction

Trait Index 80 100 120
Daughter fertility 103
Interval from calving to first insemination (cows) 96
Interval from first to last insemination (heifers) 100
Interval from first to last insemination (cows) 105
Number of inseminations (heifers) 91
Number of inseminations (cows) 101
Calving sire 102
Calving maternal 104
Udder health 113
General health 104
Longevity 108
Hoof health 106
Sole Ulcer 102
Sole Hemorrhage 102
Heel Horn Erosion 101
Digital dermatitis + Interdigital Dermatitis 116
Verrucose dermatitis + Interdigital Hyperplasia 107
Double sole + White line separation 95
Cork screw claw 101
Youngstock survival 113

NAV proof run date: 02-12-2025 Reliability 80 % Number of daughters: 1

Functional

Trait Index 80 100 120
Milkability 101
Temperament 116

NAV proof run date: 02-12-2025 Reliability 65 % Number of daughters: 0

Conformation

Trait Index 80 100 120
Frame 100
Stature 94 Short Tall
Body depth 93 Shallow Deep
Chest width 100 Narrow Wide
Rib structure 109 Coarse Angular
Top line 108 Weak Strong
Rump width 106 Narrow pins Wide pins
Rump angle 102 High pins Low pins
Feet & legs 107
Rear legs, side view 95 Straight Sickled
Rear legs, back rear view 104 Toes out Parallel, bow-legged
Foot angle 112 Low Steep
Bone quality 102 Coarse Fine and thin
Hock quality 105 Filled Dry
Udder 121
Fore udder attachment 121 Loose Strong
Rear udder height 127 Low High
Rear udder width 121 Narrow Wide
Udder support 103 Weak Strong
Udder depth 117 Deep High
Udder balance 98 Deep rear udder Deep front udder
Teat length 98 Short Long
Teat thickness 91 Thin Thick
Teat placement (front) 85 Wide Close
Teat placement (back) 105 Wide Close

NAV proof run date: 02-12-2025 Reliability 65 % Number of daughters: 0

Monogenic

Name Scientific name Symptoms Code Result
BLAD Bovine Leukocyte Adhesion Deficiency (BLF = Not carrier, BLC = Single carrier, BLS = Double carrier) BLAD is an autosomal Read more (BLF = Not carrier, BLC = Single carrier, BLS = Double carrier) BLAD is an autosomal recessively inherited defect in the Holstein population. It is characterized by recurrent bacterial infections, delayed wound healing and stunted growth. Calves with BLAD are more susceptible to infections and their lifespan varies, many die shortly after birth. Osborndale Ivanhoe (US 1189870) has been identified as the key ancestor of the disorder. Several widely used sires after Osborndale, eg. Penstate Ivanhoe Star (US 1441440) and Carlin-M Ivanhoe Bell (US 1667366) are carriers of BLAD. https://omia.org/OMIA000595/9913/ BLF Free
HH1 Holstein Haplotype 1 (HH1F = Not carrier, HH1C = Single carrier, HH1S = Double carrier) HH1 is an autosomal Read more (HH1F = Not carrier, HH1C = Single carrier, HH1S = Double carrier) HH1 is an autosomal recessively inherited defect in the Holstein population. The disorder was identified in the North American Holstein population and primarily causes early embryonic death (spontaneous abortion), but abortion can occur throughout the gestation. The key ancestor is believed to be Pawnee Farm Arlinda Chief (US1427381). https://omia.org/OMIA000001/9913/ HH1F Free
HH3 Holstein Haplotype 3 (HH3F = Not carrier, HH3C = Single carrier, HH3S = Double carrier) HH3 is an autosomal Read more (HH3F = Not carrier, HH3C = Single carrier, HH3S = Double carrier) HH3 is an autosomal recessively inherited defect in the Holstein population. The disorder has been identified in the North American and the Nordic Holstein population, however the frequency was somewhat lower in the Nordic population. HH3 primarily causes early embryonic death (spontaneous abortion), within the first 60 days of gestation. The key ancestors are believed to be Glendell Arlinda Chief (US 1556373) and Gray View Skyliner (US 1244845). https://omia.org/OMIA001824/9913/ HH3F Free
HH4 Holstein Haplotype 4 (HH4F = Not carrier, HH4C = Single carrier, HH4S = Double carrier) HH4 is an autosomal Read more (HH4F = Not carrier, HH4C = Single carrier, HH4S = Double carrier) HH4 is an autosomal recessively inherited defect in the Holstein population. The disorder was identified in the French Holstein population and causes early embryonic death (spontaneous abortion). For animals that are a heterozygous for the gene, a reduction in fertility is seen. The effect is more pronounced in heifers than cows. The key ancestor is believed to be Besne Buck (FRA 4486041658). https://omia.org/OMIA001826/9913/ HH4F Free
RP1 Progressive retinal degeneration (RP1F = Not carrier, RP1C = Single carrier, RP1S = Double carrier) Progressive retinal degeneration is Read more (RP1F = Not carrier, RP1C = Single carrier, RP1S = Double carrier) Progressive retinal degeneration is an autosomal recessively inherited defect. In the French Normande population, an association between homozygotic carrier animals of the RP1 gene and progressive blindness has been demonstrated. Blindness is due to a progressive degeneration of the photoreceptors. The RP1 mutation segregates within many cattle populations and is prevalent in e.g. the Finncattle population. For other breeds than Normande the phenotypic effect of the mutation is unclear. https://omia.org/OMIA000866/9913/ RP1F Free
HH6 Holstein Haplotype 6 (HH6F = Not carrier, HH6C = Single carrier, HH6S = Double carrier) HH6 is an autosomal Read more (HH6F = Not carrier, HH6C = Single carrier, HH6S = Double carrier) HH6 is an autosomal recessively inherited defect in the Holstein population. It was identified in the French Holstein population and causes early embryonic death (spontaneous abortion), before 35 days of gestation. The key ancestor is believed to be Gray View Skyliner (US 1244845). https://omia.org/OMIA002149/9913/ HH6F Free
HH7 Holstein Haplotype 7 (HH7F = Not carrier, HH7C = Single carrier, HH7S = Double carrier) HH7 is an autosomal Read more (HH7F = Not carrier, HH7C = Single carrier, HH7S = Double carrier) HH7 is an autosomal recessively inherited defect in the Holstein population. It was identified in the French Holstein population and causes early embryonic death (spontaneous abortion), before 35 days of gestation. https://omia.org/OMIA001830/9913/ HH7F Free

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