VH Aladdin - FRA 2912558080

Production & Efficiency

Trait Index 80 100 120
Production 121
Milk kg 106
Fat, kg 125
Fat, % 115
Protein kg 113
Protein % 108
Persistency 98
Growth 101
Daily carcass gain 102
Carcass conformation score 99
Saved feed 112
Maintenance efficiency 102

NAV proof run date: 05-05-2026 Reliability 99 % Number of daughters: 383

Expected Progeny Difference

Trait Index Bull effect Average
Milk kg, 305 days 106 196.8 11758
Fat kg, 305 days 125 31.2 487
Fat %, 305 days 115 0.24 4.2
Protein kg, 305 days 113 13.0 416
Protein %, 305 days 108 0.06 3.6

NAV proof run date: 05-05-2026 Reliability 99 % Number of daughters: 383

Health & Reproduction

Trait Index 80 100 120
Daughter fertility 104
Interval from calving to first insemination (cows) 99
Interval from first to last insemination (heifers) 99
Interval from first to last insemination (cows) 107
Number of inseminations (heifers) 89
Number of inseminations (cows) 102
Calving sire 101
Calving maternal 105
Udder health 115
General health 101
Longevity 108
Hoof health 113
Sole Ulcer 107
Sole Hemorrhage 104
Heel Horn Erosion 106
Digital dermatitis + Interdigital Dermatitis 124
Verrucose dermatitis + Interdigital Hyperplasia 110
Double sole + White line separation 99
Cork screw claw 101
Youngstock survival 110

NAV proof run date: 05-05-2026 Reliability 86 % Number of daughters: 215

Functional

Trait Index 80 100 120
Milkability 96
Temperament 114

NAV proof run date: 05-05-2026 Reliability 82 % Number of daughters: 61

Conformation

Trait Index 80 100 120
Frame 96
Stature 99 Short Tall
Body depth 91 Shallow Deep
Chest width 98 Narrow Wide
Rib structure 102 Coarse Angular
Top line 108 Weak Strong
Rump width 96 Narrow pins Wide pins
Rump angle 109 High pins Low pins
Feet & legs 110
Rear legs, side view 92 Straight Sickled
Rear legs, back rear view 105 Toes out Parallel, bow-legged
Foot angle 108 Low Steep
Bone quality 109 Coarse Fine and thin
Hock quality 109 Filled Dry
Udder 120
Fore udder attachment 121 Loose Strong
Rear udder height 128 Low High
Rear udder width 115 Narrow Wide
Udder support 104 Weak Strong
Udder depth 115 Deep High
Udder balance 97 Deep rear udder Deep front udder
Teat length 94 Short Long
Teat thickness 87 Thin Thick
Teat placement (front) 89 Wide Close
Teat placement (back) 102 Wide Close

NAV proof run date: 05-05-2026 Reliability 82 % Number of daughters: 61

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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