Other breed-specific considerations
Breed: Clumber Spaniel
Breeds in this Condition
Breeds
Condition
Other breed-specific considerations
Synonym
Andere rassespezifische Überlegungen,Autres considérations spécifiques à la race / Autres considérations propres à la race,Andra rasspecifika överväganden,Muuta rotukohtaista huomioitavaa,Andere rasspecifieke overwegingen
Test Types(s)
various
Type
Condition; Disease/ disorder
Breed-specific 1 details
Breed-specific 2 Details
HSP Test-Specific Data
Swedish Clumber Spaniel Club
HSP
HSP Name 2
Clumber Spaniel Klubben
Breed
Condition
Specific Condition[s]
Acanthosis nigricans; Basenji Spring collapse; Bladder Stones ; Body condition ; Breed type; Canine idiopathic pulmonary fibrosis/ CIPF; canine thrombopathy/ CTP; Charcot-Marie-Tooth Neuropathy/ CMT; Chronic Active Hepatitis/ CAH; Chronic Hepatitis/ CH; Closed ears; Copper Toxicosis/ COMMD-1; Cutaneous Mucinosis; Dandy-Walker-Like-Malformation/ DWLM; Ear lobe vasculitis/ Cutaneous vasculitis ; Elbow luxation; Factor XI deficiency; Fibrocartilaginous Emboli/ FCE; Gallbladder mucocele/ GBM; GM1-gangliosidosis; health compilation; Hepatic Microvascular dysplasia/ MVD; Hereditary Nephritis; Hypoglycemia; idiopathic facial nerve paralysis/ Facial paralysis; Imerslund-Gräsbäck syndrome/ IGS; Immunoproliferative enteropathy/ IPSID; Improper Coat; Inherited Myelodysplacia of Weimaraners/ Myelodysplacia; Inherited pancreatitis; Ivermectin Toxicity; Juvenile Hereditary cataracts/ HC-HSF4; Juvenile Renal Dysplasia/ Juvenile Nephropathy-; Keratoacanthoma; L-2-hydroxyglutaric aciduria/ L-2-HGA; Lagotto Storage Disease/ LSD; Leonberger Polyneuropathy/ LPN; Lethal acrodermatitis Bull Terrier Type/LAD; Lethal Lung Disease/ LAMP3; Leukoencephalomyepathy/ LEMP; Long soft palate / Reverse sneezing; Low resistance to infection, pneumonia; Low Uric Acid/ LUA; Lundehund Syndrome/ Intestinal lymphangiectasia; membranoproliferative glomerulonephritis/ MPGN ; Mucopolysaccharidosis (Sanfilippo syndrome)/MPSIIIB; Mucopolysaccharidosis VII Brazilian Terrier Type/ MPS VII; Muscular Dystrophy (Duchenne-type, DMD) GRMD; Muscular Dystrophy DM; Mycobacterium Avium complex MAC; Mycobacterium Avium complex/MAC; Myotonia Congenita; Neuroaxonal Dystrophy/ NAD; Neuronal Degeneration/ NDG; Norwich Terrier Upper Airway Syndrome/ NTUAS; Oculocutaneous albinism/ OCA2; Osteogenesis imperfecta/ OI; Persistent Müllerian Duct Syndrome/ PMDS; Pes Varus; Pinnal Alopecia; Pinnal Alopecia; Polycystic kidney disease/ PKD/PCD ; Polyneuropathy ; Portacaval shunts ; Post-vaccinal reaction; Pulmonary edema; Pyruvate dehydrogenase phosphate 1 deficiency/ PDP1; Samoyed hereditary glomerulopathy/ SHG; Shaking Legs/postural tremors; Skin damage of unethical shaving; SPAID-gene test; Spondylocostal dysostosis/Comma defect/ SCD; Thrombocytopenia/TUBB1; macrothrombocytopenia; Trapped Neutrophil Syndrome/TNS; Van den Ende?Gupta Syndrome/ VDEGS;
Breed-specific Condition Descripton
Pyruvate dehydrogenase phosphate 1 deficiency/ PDP1
Specific test type(s)
genetic/genomic
Required Comment
-
Recommended
Recommended Comment
-
Recognized Comment
-
Date
02/03/2023 07:37 PM
Country
Sweden
Country code
SE
Additional Information
Finnish Spaniel Association
HSP
HSP Name 2
Suomen Spanieliliitto - Finlands Spanielförbund ry
Breed
Condition
Specific Condition[s]
Acanthosis nigricans; Basenji Spring collapse; Bladder Stones ; Body condition ; Breed type; Canine idiopathic pulmonary fibrosis/ CIPF; canine thrombopathy/ CTP; Charcot-Marie-Tooth Neuropathy/ CMT; Chronic Active Hepatitis/ CAH; Chronic Hepatitis/ CH; Closed ears; Copper Toxicosis/ COMMD-1; Cutaneous Mucinosis; Dandy-Walker-Like-Malformation/ DWLM; Ear lobe vasculitis/ Cutaneous vasculitis ; Elbow luxation; Factor XI deficiency; Fibrocartilaginous Emboli/ FCE; Gallbladder mucocele/ GBM; GM1-gangliosidosis; health compilation; Hepatic Microvascular dysplasia/ MVD; Hereditary Nephritis; Hypoglycemia; idiopathic facial nerve paralysis/ Facial paralysis; Imerslund-Gräsbäck syndrome/ IGS; Immunoproliferative enteropathy/ IPSID; Improper Coat; Inherited Myelodysplacia of Weimaraners/ Myelodysplacia; Inherited pancreatitis; Ivermectin Toxicity; Juvenile Hereditary cataracts/ HC-HSF4; Juvenile Renal Dysplasia/ Juvenile Nephropathy-; Keratoacanthoma; L-2-hydroxyglutaric aciduria/ L-2-HGA; Lagotto Storage Disease/ LSD; Leonberger Polyneuropathy/ LPN; Lethal acrodermatitis Bull Terrier Type/LAD; Lethal Lung Disease/ LAMP3; Leukoencephalomyepathy/ LEMP; Long soft palate / Reverse sneezing; Low resistance to infection, pneumonia; Low Uric Acid/ LUA; Lundehund Syndrome/ Intestinal lymphangiectasia; membranoproliferative glomerulonephritis/ MPGN ; Mucopolysaccharidosis (Sanfilippo syndrome)/MPSIIIB; Mucopolysaccharidosis VII Brazilian Terrier Type/ MPS VII; Muscular Dystrophy (Duchenne-type, DMD) GRMD; Muscular Dystrophy DM; Mycobacterium Avium complex MAC; Mycobacterium Avium complex/MAC; Myotonia Congenita; Neuroaxonal Dystrophy/ NAD; Neuronal Degeneration/ NDG; Norwich Terrier Upper Airway Syndrome/ NTUAS; Oculocutaneous albinism/ OCA2; Osteogenesis imperfecta/ OI; Persistent Müllerian Duct Syndrome/ PMDS; Pes Varus; Pinnal Alopecia; Pinnal Alopecia; Polycystic kidney disease/ PKD/PCD ; Polyneuropathy ; Portacaval shunts ; Post-vaccinal reaction; Pulmonary edema; Pyruvate dehydrogenase phosphate 1 deficiency/ PDP1; Samoyed hereditary glomerulopathy/ SHG; Shaking Legs/postural tremors; Skin damage of unethical shaving; SPAID-gene test; Spondylocostal dysostosis/Comma defect/ SCD; Thrombocytopenia/TUBB1; macrothrombocytopenia; Trapped Neutrophil Syndrome/TNS; Van den Ende?Gupta Syndrome/ VDEGS;
Breed-specific Condition Descripton
Pyruvate dehydrogenase phosphate 1 deficiency/ PDP1
Specific test type(s)
genetic/genomic
Required by HSP
Required Comment
not to combine two carriers
Recommended Comment
-
Recognized Comment
-
Date
02/03/2023 07:37 PM
Country
Finland
Country code
FI
Additional Information
Finnish Kennel Club
HSP
HSP Name 2
Suomen Kennelliitto
Breed
Condition
Specific Condition[s]
Acanthosis nigricans; Basenji Spring collapse; Bladder Stones ; Body condition ; Breed type; Canine idiopathic pulmonary fibrosis/ CIPF; canine thrombopathy/ CTP; Charcot-Marie-Tooth Neuropathy/ CMT; Chronic Active Hepatitis/ CAH; Chronic Hepatitis/ CH; Closed ears; Copper Toxicosis/ COMMD-1; Cutaneous Mucinosis; Dandy-Walker-Like-Malformation/ DWLM; Ear lobe vasculitis/ Cutaneous vasculitis ; Elbow luxation; Factor XI deficiency; Fibrocartilaginous Emboli/ FCE; Gallbladder mucocele/ GBM; GM1-gangliosidosis; health compilation; Hepatic Microvascular dysplasia/ MVD; Hereditary Nephritis; Hypoglycemia; idiopathic facial nerve paralysis/ Facial paralysis; Imerslund-Gräsbäck syndrome/ IGS; Immunoproliferative enteropathy/ IPSID; Improper Coat; Inherited Myelodysplacia of Weimaraners/ Myelodysplacia; Inherited pancreatitis; Ivermectin Toxicity; Juvenile Hereditary cataracts/ HC-HSF4; Juvenile Renal Dysplasia/ Juvenile Nephropathy-; Keratoacanthoma; L-2-hydroxyglutaric aciduria/ L-2-HGA; Lagotto Storage Disease/ LSD; Leonberger Polyneuropathy/ LPN; Lethal acrodermatitis Bull Terrier Type/LAD; Lethal Lung Disease/ LAMP3; Leukoencephalomyepathy/ LEMP; Long soft palate / Reverse sneezing; Low resistance to infection, pneumonia; Low Uric Acid/ LUA; Lundehund Syndrome/ Intestinal lymphangiectasia; membranoproliferative glomerulonephritis/ MPGN ; Mucopolysaccharidosis (Sanfilippo syndrome)/MPSIIIB; Mucopolysaccharidosis VII Brazilian Terrier Type/ MPS VII; Muscular Dystrophy (Duchenne-type, DMD) GRMD; Muscular Dystrophy DM; Mycobacterium Avium complex MAC; Mycobacterium Avium complex/MAC; Myotonia Congenita; Neuroaxonal Dystrophy/ NAD; Neuronal Degeneration/ NDG; Norwich Terrier Upper Airway Syndrome/ NTUAS; Oculocutaneous albinism/ OCA2; Osteogenesis imperfecta/ OI; Persistent Müllerian Duct Syndrome/ PMDS; Pes Varus; Pinnal Alopecia; Pinnal Alopecia; Polycystic kidney disease/ PKD/PCD ; Polyneuropathy ; Portacaval shunts ; Post-vaccinal reaction; Pulmonary edema; Pyruvate dehydrogenase phosphate 1 deficiency/ PDP1; Samoyed hereditary glomerulopathy/ SHG; Shaking Legs/postural tremors; Skin damage of unethical shaving; SPAID-gene test; Spondylocostal dysostosis/Comma defect/ SCD; Thrombocytopenia/TUBB1; macrothrombocytopenia; Trapped Neutrophil Syndrome/TNS; Van den Ende?Gupta Syndrome/ VDEGS;
Breed-specific Condition Descripton
Pyruvate dehydrogenase phosphate 1 deficiency/ PDP1
Specific test type(s)
genetic/genomic
Required by HSP
Required Comment
not to combine two carriers
Recommended Comment
-
Recognized Comment
-
Date
02/03/2023 07:37 PM
Country
Finland
Country code
FI
Additional Information