Beau-Batu von der Weizenfelder

100 lbs

Beau has MANY generations of our Amazing Lines!

Many of the dogs seen here in years past are included in his pedigree:

Django von der Weizenfelder, 
Apollo von der Weizenfelder, 
Royal Zena von Fleischerhiem,  
Meiko vom Zellwaldrand & 
Roxi vom Mystical Haus!

Take a look, Pedigree Below:
(Link to extended PEDIGREE Above)

Beau is OFA Certified with: Good HIPS

We will be seeing some litters out of Beau starting in 2023.

Beau is a very protective boy. 
He also has the mass to back it up. 
However, he is medium Drive.

Beau is Wisdom Panel Clear all traits / diseases they test for. 
Including DM CLEAR!

A lot of the tests with Wisdom Panel target other breeds and do not technically pose a risk to the German Shepherd. 

However, I will list below the ones that could pose a risk.

More tests than are listed below were tested for, and all were CLEAR on the full panel for Beau!


Acral Mutilation Syndrome

Acute Respiratory Distress Syndrome

Alexander Disease

Bandera’s Neonatal Ataxia

Benign Familial Juvenile Epilepsy

Canine Leukocyte Adhesion Deficiency aka (CLAD) Type III

Canine Multifocal Retinopathy 1, 2 and 3

Canine Scott Syndrome

Cerebellar Ataxia

Cerebellar Cortical Degeneration

Cerebellar Hypoplasia

Cerebral Dysfunction

Cleft Lip & Palate (Also CL&P with Syndactyly)

Complement 3 Deficiency

Cone Degeneration

Cone-Rod Dystrophy

Congenital Stationary Night Blindness aka (CSNB)

Cystic Renal Dysplasia and Hepatic Fibrosis

Cystinuria Type I-A & II-A

(DM) aka Degenerative Myelopathy

Dental Hypomineralization

Dominant Progressive Retinal Atrophy (DPRA)

Epidermolytic Hyperkeratosis

Episodic Falling Syndrome (EFS)

Exercise-Induced Collapse (EIC)

Factor VII, XI Syndrome

Fanconi Syndrome

Fetal Onset Neuroaxonal Dystrophy

Focal Non-Epidermolytic Palmoplantar Keratoderma

Glycogen Storage Disease Type IIIa (GSD IIIa)

Hemophilia A – Variant’s 1 & (2-German Shepherd Dog)

Hemophilia B

Hereditary Elliptocytosis

Hereditary Footpad Hyperkeratosis (HFH)

Hereditary Vitamin D-Resistant Rickets Type II (HVDRR)

Hyperuricosuria (HUU)




Juvenile Laryngeal Paralysis and Polyneuropathy (JLPP)

Juvenile Myoclonic Epilepsy

Lagotto Storage Disease

Lamellar Ichthyosis

Ligneous Membranitis

MDR1 Medication Sensitivity (MDR1)

May-Hegglin Anomaly

Mucopolysaccharidosis Type VII (Discovered in the German Shepherd Dog)

Muscular Hypertrophy (Double Muscling)

Musladin-Lueke Syndrome

Myeloperoxidase Deficiency

Myotubular Myopathy

Nemaline Myopathy

Neonatal Cerebellar Cortical Degeneration

Neonatal Encephalopathy with Seizures

Neuronal Ceroid Lipofuscinosis 1 (NCL1)

Neuronal Ceroid Lipofuscinosis 7 (NCL7)

Obesity Risk (Pomc)


P2RY12- Associated Bleeding Disorder

Paroxysmal Dyskinesia

Persistent Mullerian Duct Syndrome (PMDS)

Phosphofructokinase Deficiency (PKF)

Polycystic Kidney Disease (PKD)

Primary Ciliary Dyskinesia

Primary Lens Luxation

Progressive Early-Onset Cerebellar Ataxia

Progressive Retinal Atrophy III, and 1 (PRA)

Progressive Rod Cone Degeneration (prcd-pra)

Protein Losing Nephropathy

Pyruvate Dehydrogenase Phosphatase 1 Deficiency (PDP1)

QT Syndrome (LQTS)

Renal Cystadenocarcinoma and Nodular Dermatofibrosis

Rode-Cone Dysplasia (1, 1a & 3)

Sensory Ataxic Neuropathy (SAN)

Sensory Neuropathy

Skeletal Dysplasia 2

Spinocerebellar Ataxia (Late onset Ataxia) (LOA)

Spinocerebellar Ataxia with Myokymia and / or Seizures (SAMS)

Spondylocostal Dysostosis

Spongy Degeneration with Cerebellar Ataxia (SDCA1) (SDCA2)

Trapped Neutrophil Syndrome

X-Linked Ectodermal Dysplasia

X-Linked Myotubular Myopathy (XLMTM)

X-Linked Progressive Retinal Atrophy 1 & 2 (XLPRA1) (XLPRA2)

X-Linked Tremors

Von Willebrand’s Disease (Type 1,2 and 3) (vWD)