VH Harry P - DEU 361199175

Production & Efficiency

Trait Index 80 100 120
Production 103
Milk kg 90
Fat, kg 101
Fat, % 110
Protein kg 100
Protein % 116
Persistency 99
Growth 92
Daily carcass gain 94
Carcass conformation score 92
Saved feed 95
Maintenance efficiency 93

NAV proof run date: 04-11-2025 Reliability 99 % Number of daughters: 7022

Expected Progeny Difference

Trait Index Bull effect Average
Milk kg, 305 days 90 -328.1 11600
Fat kg, 305 days 101 1.2 475
Fat %, 305 days 110 0.16 4.1
Protein kg, 305 days 100 0.0 406
Protein %, 305 days 116 0.12 3.5

NAV proof run date: 04-11-2025 Reliability 99 % Number of daughters: 7022

Health & Reproduction

Trait Index 80 100 120
Daughter fertility 109
Calving sire 106
Calving maternal 99
Udder health 101
General health 107
Longevity 105
Hoof health 106
Sole Ulcer 102
Sole Hemorrhage 103
Heel Horn Erosion 102
Digital dermatitis + Interdigital Dermatitis 116
Verrucose dermatitis + Interdigital Hyperplasia 105
Double sole + White line separation 108
Cork screw claw 114
Youngstock survival 107

NAV proof run date: 04-11-2025 Reliability 99 % Number of daughters: 6550

Functional

Trait Index 80 100 120
Milkability 108
Temperament 102

NAV proof run date: 04-11-2025 Reliability 97 % Number of daughters: 2818

Conformation

Trait Index 80 100 120
Frame 101
Stature 100 Short Tall
Body depth 107 Shallow Deep
Chest width 96 Narrow Wide
Rib structure 97 Coarse Angular
Top line 88 Weak Strong
Rump width 103 Narrow pins Wide pins
Rump angle 98 High pins Low pins
Feet & legs 105
Rear legs, side view 90 Straight Sickled
Rear legs, back rear view 112 Toes out Parallel, bow-legged
Foot angle 90 Low Steep
Bone quality 102 Coarse Fine and thin
Hock quality 108 Filled Dry
Udder 92
Fore udder attachment 95 Loose Strong
Rear udder height 96 Low High
Rear udder width 100 Narrow Wide
Udder support 105 Weak Strong
Udder depth 104 Deep High
Udder balance 114 Deep rear udder Deep front udder
Teat length 102 Short Long
Teat thickness 103 Thin Thick
Teat placement (front) 100 Wide Close
Teat placement (back) 115 Wide Close

NAV proof run date: 04-11-2025 Reliability 97 % Number of daughters: 2818

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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