VH Aladdin - FRA 2912558080

Production & Efficiency

Trait Index 80 100 120
Production 125
Milk kg 109
Fat, kg 128
Fat, % 115
Protein kg 116
Protein % 108
Persistency 96
Growth 101
Daily carcass gain 103
Carcass conformation score 98
Saved feed 102
Maintenance efficiency 111

NAV proof run date: 03-02-2026 Reliability 96 % Number of daughters: 65

Expected Progeny Difference

Trait Index Bull effect Average
Milk kg, 305 days 109 295.3 11702
Fat kg, 305 days 128 35.0 483
Fat %, 305 days 115 0.24 4.2
Protein kg, 305 days 116 16.0 413
Protein %, 305 days 108 0.06 3.5

NAV proof run date: 03-02-2026 Reliability 96 % Number of daughters: 65

Health & Reproduction

Trait Index 80 100 120
Daughter fertility 103
Interval from calving to first insemination (cows) 98
Interval from first to last insemination (heifers) 98
Interval from first to last insemination (cows) 105
Number of inseminations (heifers) 88
Number of inseminations (cows) 101
Calving sire 101
Calving maternal 105
Udder health 120
General health 105
Longevity 108
Hoof health 105
Sole Ulcer 103
Sole Hemorrhage 100
Heel Horn Erosion 98
Digital dermatitis + Interdigital Dermatitis 114
Verrucose dermatitis + Interdigital Hyperplasia 103
Double sole + White line separation 94
Cork screw claw 100
Youngstock survival 112

NAV proof run date: 03-02-2026 Reliability 88 % Number of daughters: 31

Functional

Trait Index 80 100 120
Milkability 99
Temperament 115

NAV proof run date: 03-02-2026 Reliability 71 % Number of daughters: 10

Conformation

Trait Index 80 100 120
Frame 97
Stature 96 Short Tall
Body depth 91 Shallow Deep
Chest width 97 Narrow Wide
Rib structure 106 Coarse Angular
Top line 107 Weak Strong
Rump width 103 Narrow pins Wide pins
Rump angle 106 High pins Low pins
Feet & legs 109
Rear legs, side view 96 Straight Sickled
Rear legs, back rear view 104 Toes out Parallel, bow-legged
Foot angle 114 Low Steep
Bone quality 105 Coarse Fine and thin
Hock quality 105 Filled Dry
Udder 124
Fore udder attachment 119 Loose Strong
Rear udder height 129 Low High
Rear udder width 119 Narrow Wide
Udder support 104 Weak Strong
Udder depth 117 Deep High
Udder balance 96 Deep rear udder Deep front udder
Teat length 102 Short Long
Teat thickness 92 Thin Thick
Teat placement (front) 88 Wide Close
Teat placement (back) 102 Wide Close

NAV proof run date: 03-02-2026 Reliability 71 % Number of daughters: 10

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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