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IMG New Packaging Breed Health for Cats

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Browse Cat Traits

Main Cat Traits

Cat Traits

Coat color and pattern

White feet

Congenital myasthenic syndrome, COLQ-related

Congenital muscular dystrophy, LAMA2-related

Cataracts, FYCO1-related

Intestinal lipid malabsorption

Primary open angle glaucoma (POAG), ADAMTS17-related

Dental-skeletal-retinal anomaly (DSRA)

Congenital cornification disorder

Arrhythmogenic right ventricular cardiomyopathy (ARVC)

Nemaline myopathy

Osteochondrodysplasia

Vitamin D-deficiency rickets, type II

Exfoliative cutaneous lupus erythematosus (ECLE)

Sensory ataxic neuropathy

Ichthyosis, TGM1-related

Pancreatitis, SPINK1-related

Paroxysmal dyskinesia, SOD1-related

Cerebellar cortical degeneration

Hyperekplexia

Spinocerebellar ataxia, SLC12A6-related

CNS atrophy and cerebellar ataxia

Van den Ende-Gupta syndrome

Polyneuropathy, SBF2-related

Leber congenital amaurosis

Rod-cone dysplasia 2 (rcd2)

Microphthalmia with coloboma

Laryngeal paralysis, RAPGEF6-related

Colorectal hamartomatous polyposis and ganglioneuromatosis

Progressive retinal atrophy, PPT1-related

Ectodermal dysplasia - skin fragility syndrome (ED-SFS)

Paroxysmal dyskinesia, PIGN-related

Rod-cone dysplasia 1a (rcd1a), PDB Beta subunit-related

XY disorder of sexual development, NR5A1-related

Cone-rod dystrophy, NPHP4-related

Spinal dysraphism

Ichthyosis, NIPAL4-related

Myoclonus epilepsy of Lafora

Collie eye anomaly

Myeloperoxidase deficiency

Fetal-onset neuroaxonal dystrophy, MFN2-related

Progressive Retinal Atrophy, MERTK-related

Macular corneal dystrophy

Focal non-epidermolytic palmoplantar keratoderma

Squamous cell carcinoma of the digit

Spinocerebellar ataxia, ITPR1-related

Progressive Retinal Atrophy, IMPG2-related

Cataract, HSF4-related

Periodic Fever Syndrome 1

Bernard-Soulier syndrome, type C

Acral mutilation syndrome

Fucosidosis

Canine ectodermal dysplasia (CED)

Intervertebral disc disease, type I

Ridge and dermoid sinus

Chondrodystrophy and intervertebral disc disease

Afibrinogenaemia

Progressive retinal atrophy, FAM161A-related

Osteochondromatosis

Labrador Retriever muscular dystrophy (LRMD)

Cleft palate

Leukodystrophy, CYTB-related

Reduced ability to metabolize cognitive enhancer 5-(3-methoxyphenyl)-3-(5-methyl1,2,4-oxadiazol-3-yl)-2-oxo-1,2-dihydro-1,6-naphthyridine (AC-3933)

Wilson's disease, COMMD1-related

Oculoskeletal dysplasia, COL9A2-related

Ehlers-Danlos syndrome, classic type

Rod-cone dysplasia 4 (rcd4)

XX disorder of sexual development (testicular and ovotesticular subtype), BTBD17-related

Episodic falling syndrome (EFS)

Neuronal ceroid lipofuscinosis, CTSD-related

Cone-rod dystrophy 3 (crd3)

Obesity

Amelogenesis imperfecta, ACP4-related

Fanconi syndrome

Mucopolysaccharidosis IIIB

Mucopolysaccharidosis I

Upper airway syndrome

Cleft lip with or without cleft palate

Neutropenia

Imerslund-Gräsbeck syndrome, AMN-related

Gallbladder mucoceles

Darier disease

Dwarfism, POU1F1-related

Rod-Cone Dysplasia (Rdy)

Spinal Muscular Atrophy (SMA)

Congenital Myasthenic Syndrome (CMS)

Brachycephaly, Burmese Head Defect

Holoprosencephaly

Merle coat (general)

Recessive black coat color

White-spotted coat color

White coat color

Mocha coat color

Dwarfism

Height

Polydactyly

Blue eyes and heterochromia

White-spotted coat (Piebald)

Albinism, OCA2-related

Cryptic merle coat

White-spotted coat (extreme white)