Moe Chocolate Male Stud
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Moe is a chocolate English male. chocolate labrador puppy, lab puppies for sale st. louis labrador puppies
We have listed the testing we added to him below. chocolate labrador puppy lab puppies for sale st. louis labrador puppies
He is also tested for the diseases listed on our Genetic testing page. chocolate labrador puppy lab puppies for sale st. louis labrador puppies
He is our most extensively tested male to date. chocolate labrador puppy lab puppies for sale st. louis labrador puppies
Moe is one of the funniest dogs. He has this clown attitude that will make your day if you are needing cheered up. He is one that loves attention and loves to cuddle. chocolate labrador puppy lab puppies for sale st. louis labrador puppies
We are extremely happy with him and hope he is happy to live here with us. He does let us know when a stranger is here, and then will proceed to lick that stranger after his very deep bark.
We’ve never had any issue of aggression out of him with any humans or animals. He’s just a very happy goofy large boy.
Loves to fetch and toss toys around. He loves the water and swims any chance he gets.
We really hope if you get one of his puppies that they will be a part of your family for a long time.
The picture below is of a puppy from his first litter. Born in 2019 nine months old in photo. chocolate labrador puppy lab puppies for sale st. louis labrador puppies
chocolate labrador puppy lab puppies for sale st. louis labrador puppies
Moe was tested for the following diseases and we are happy to report he was clear on all of them. chocolate labrador puppy lab puppies for sale st. louis labrador puppies
- Coagulation factor VII deficiency
- Elliptocytosis
- Leukocyte adhesion deficiency, type III
- May-Hegglin anomaly
- P2RY12 receptor platelet disorder
- Prekallikrein deficiency
- Pyruvate kinase deficiency
- Von Willebrand disease
- Renal cystadenocarcinoma and nodular dermatofibrosis
- Amelogenesis imperfecta
- Multidrug resistance 1
- Cone degeneration
- Congenital stationary night blindness
- Dry eye curly coat syndrome
- Early retinal degeneration
- Hereditary cataracts
- Juvenile Laryngeal Paralysis and Polyneuropathy
- Multifocal retinopathy 1
- Multifocal retinopathy 2
- Multifocal retinopathy 3
- Primary lens luxation
- Primary open angle glaucoma
- Progressive retinal atrophy, Cone-rod dystrophy
- Progressive retinal atrophy
- Progressive rod-cone degeneration
- Progressive retinal atrophy Rod-cone dysplasia 3
- Progressive retinal atrophy, generalized
- Complement 3 deficiency
- Primary ciliary dyskinesia
- Trapped neutrophil syndrome
- Gallbladder mucoceles
- Glycogen storage disease IIIa
- Adult-onset neuronal ceroid lipofuscinosis
- Glycogen storage disease IIIa
- Glycogen storage disease Ia
- Glycogen storage disease VII
- Mucopolysaccharidosis I
- Neuronal ceroid lipofuscinosis 1
- Neuronal ceroid lipofuscinosis 10
- Neuronal ceroid lipofuscinosis 2
- Neuronal ceroid lipofuscinosis 4A
- Neuronal ceroid lipofuscinosis 5
- Neuronal ceroid lipofuscinosis 6
- Pompe disease
- Pyruvate dehydrogenase deficiency
- Pyruvate kinase deficiency
- Juvenile Laryngeal Paralysis and Polyneuropathy
- Adult-onset neuronal ceroid lipofuscinosis
- Congenital myasthenic syndrome
- Degenerative myelopathy
- Exercise-induced collapse
- Glycogen storage disease IIIa
- Juvenile Laryngeal Paralysis and Polyneuropathy
- Mucopolysaccharidosis I
- Musladin-Lueke syndrome
- Myotubular myopathy 1
- Osteochondrodysplasia
- Pompe disease
- Skeletal dysplasia 2
- Adult-onset neuronal ceroid lipofuscinosis
- Benign familial juvenile epilepsy
- Congenital myasthenic syndrome
- Degenerative myelopathy
- Episodic falling syndrome
- Exercise-induced collapse
- Juvenile Laryngeal Paralysis and Polyneuropathy
- Late onset ataxia
- Mucopolysaccharidosis I
- Musladin-Lueke syndrome
- Narcolepsy
- Neonatal cerebellar cortical degeneration
- Neonatal encephalopathy with seizures
- Neuronal ceroid lipofuscinosis 1
- Neuronal ceroid lipofuscinosis 10
- Neuronal ceroid lipofuscinosis 2
- Neuronal ceroid lipofuscinosis 4A
- Neuronal ceroid lipofuscinosis 5
- Neuronal ceroid lipofuscinosis 6
- Sensory ataxic neuropathy
- Spinocerebellar ataxia
- Startle disease
- Primary ciliary dyskinesia
- Primary ciliary dyskinesia
- Anhidrotic ectodermal dysplasia
- Dry eye curly coat syndrome
- Dystrophic epidermolysis bullosa
- Ectodermal dysplasia
- Epidermolytic hyperkeratosis
- Hereditary nasal parakeratosis
- Renal cystadenocarcinoma and nodular dermatofibrosis
- Fanconi syndrome
- Hyperuricosuria
- Persistent Müllerian duct syndrome
- Primary ciliary dyskinesia
- Primary hyperoxaluria
- Renal cystadenocarcinoma and nodular dermatofibrosis
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