VH Aladdin - FRA 2912558080

Production & Efficiency

Trait Index 80 100 120
Production 118
Milk kg 102
Fat, kg 123
Fat, % 116
Protein kg 109
Protein % 109
Persistency 96
Growth 100
Daily carcass gain 101
Carcass conformation score 98
Saved feed 112
Maintenance efficiency 106

NAV proof run date: 11-08-2026 Reliability 99 % Number of daughters: 1181

Expected Progeny Difference

Trait Index Bull effect Average
Milk kg, 305 days 102 65.6 11758
Fat kg, 305 days 123 28.7 487
Fat %, 305 days 116 0.26 4.2
Protein kg, 305 days 109 9.0 416
Protein %, 305 days 109 0.07 3.6

NAV proof run date: 11-08-2026 Reliability 99 % Number of daughters: 1181

Health & Reproduction

Trait Index 80 100 120
Daughter fertility 109
Interval from calving to first insemination (cows) 101
Interval from first to last insemination (heifers) 99
Interval from first to last insemination (cows) 112
Number of inseminations (heifers) 89
Number of inseminations (cows) 105
Calving sire 101
Calving maternal 107
Udder health 110
General health 98
Longevity 109
Hoof health 113
Sole Ulcer 108
Sole Hemorrhage 109
Heel Horn Erosion 107
Digital dermatitis + Interdigital Dermatitis 121
Verrucose dermatitis + Interdigital Hyperplasia 106
Double sole + White line separation 107
Cork screw claw 106
Youngstock survival 110

NAV proof run date: 11-08-2026 Reliability 95 % Number of daughters: 898

Functional

Trait Index 80 100 120
Milkability 98
Temperament 111

NAV proof run date: 11-08-2026 Reliability 87 % Number of daughters: 278

Conformation

Trait Index 80 100 120
Frame 91
Stature 96 Short Tall
Body depth 85 Shallow Deep
Chest width 94 Narrow Wide
Rib structure 99 Coarse Angular
Top line 102 Weak Strong
Rump width 95 Narrow pins Wide pins
Rump angle 110 High pins Low pins
Feet & legs 113
Rear legs, side view 94 Straight Sickled
Rear legs, back rear view 110 Toes out Parallel, bow-legged
Foot angle 109 Low Steep
Bone quality 113 Coarse Fine and thin
Hock quality 106 Filled Dry
Udder 121
Fore udder attachment 119 Loose Strong
Rear udder height 126 Low High
Rear udder width 117 Narrow Wide
Udder support 100 Weak Strong
Udder depth 116 Deep High
Udder balance 96 Deep rear udder Deep front udder
Teat length 103 Short Long
Teat thickness 92 Thin Thick
Teat placement (front) 88 Wide Close
Teat placement (back) 100 Wide Close

NAV proof run date: 11-08-2026 Reliability 87 % Number of daughters: 278

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