VH Larfelt - DNK 260212 - VikingHolstein

Production & Efficiency

Trait Index 80 100 120
Production 99
Milk kg 93
Fat, kg 98
Fat, % 104
Protein kg 98
Protein % 109
Persistency 94
Growth 99
Daily carcass gain 95
Carcass conformation score 103
Saved feed 108
Maintenance efficiency 94

NAV proof run date: 03-11-2026 Reliability 98 % Number of daughters: 236

Expected Progeny Difference

Trait Index Bull effect Average
Milk lbs, 305 days 93 -506.18 25,921.95
Fat lbs, 305 days 98 -5.51 1,073.65
Fat %, 305 days 104 0.06 4.2
Protein lbs, 305 days 98 -4.41 917.12
Protein %, 305 days 109 0.07 3.6

NAV proof run date: 03-11-2026 Reliability 98 % Number of daughters: 236

Health & Reproduction

Trait Index 80 100 120
Daughter fertility 106
Interval from calving to first insemination (cows) 106
Interval from first to last insemination (heifers) 97
Interval from first to last insemination (cows) 106
Number of inseminations (heifers) 97
Number of inseminations (cows) 104
Calving sire 104
Calving maternal 100
Udder health 100
General health 107
Longevity 109
Hoof health 110
Sole Ulcer 105
Sole Hemorrhage 109
Heel Horn Erosion 112
Digital dermatitis + Interdigital Dermatitis 120
Verrucose dermatitis + Interdigital Hyperplasia 99
Double sole + White line separation 95
Cork screw claw 105
Youngstock survival 112

NAV proof run date: 03-11-2026 Reliability 94 % Number of daughters: 229

Functional

Trait Index 80 100 120
Milkability 105
Temperament 101

NAV proof run date: 03-11-2026 Reliability 84 % Number of daughters: 50

Conformation

Trait Index 80 100 120
Frame 103
Stature 91 Short Tall
Body depth 108 Shallow Deep
Chest width 117 Narrow Wide
Rib structure 93 Coarse Angular
Top line 102 Weak Strong
Rump width 101 Narrow pins Wide pins
Rump angle 99 High pins Low pins
Feet & legs 86
Rear legs, side view 77 Straight Sickled
Rear legs, back rear view 99 Toes out Parallel, bow-legged
Foot angle 108 Low Steep
Bone quality 89 Coarse Fine and thin
Hock quality 82 Filled Dry
Udder 101
Fore udder attachment 111 Loose Strong
Rear udder height 109 Low High
Rear udder width 111 Narrow Wide
Udder support 97 Weak Strong
Udder depth 91 Deep High
Udder balance 116 Deep rear udder Deep front udder
Teat length 103 Short Long
Teat thickness 113 Thin Thick
Teat placement (front) 95 Wide Close
Teat placement (back) 93 Wide Close

NAV proof run date: 03-11-2026 Reliability 84 % Number of daughters: 50

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