Conditions related to genes on chromosome 19

Genetics Home Reference includes these conditions related to genes on chromosome 19:

• age-related macular degeneration
• Aicardi-Goutieres syndrome
• alpha-mannosidosis
• Alzheimer disease
• atypical hemolytic-uremic syndrome
• branchiootorenal syndrome
• breast cancer
• Camurati-Engelmann disease
• cardiofaciocutaneous syndrome
• Carpenter syndrome
• central core disease
• centronuclear myopathy
• cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy
• Charcot-Marie-Tooth disease
• Coffin-Siris syndrome
• cold-induced sweating syndrome
• congenital fiber-type disproportion
• congenital hypothyroidism
• cyclic neutropenia
• cystinuria
• dense deposit disease
• Diamond-Blackfan anemia
• episodic ataxia
• ethylmalonic encephalopathy
• familial acute myeloid leukemia with mutated CEBPA
• familial cold autoinflammatory syndrome
• familial erythrocytosis
• familial hemiplegic migraine
• familial hypertrophic cardiomyopathy
• familial restrictive cardiomyopathy
• glutaric acidemia type I
• glutaric acidemia type II
• guanidinoacetate methyltransferase deficiency
• hemochromatosis
• hereditary sensory and autonomic neuropathy type IE
• hypercholesterolemia
• hyperferritinemia-cataract syndrome
• Kawasaki disease
• malignant hyperthermia
• maple syrup urine disease
• 3-methylglutaconic aciduria
• mucolipidosis type IV
• multiminicore disease
• multiple epiphyseal dysplasia
• myotonic dystrophy
• neuroferritinopathy
• persistent Müllerian duct syndrome
• Peutz-Jeghers syndrome
• polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy
• pontocerebellar hypoplasia
• prolidase deficiency
• pseudoachondroplasia
• rapid-onset dystonia parkinsonism
• severe congenital neutropenia
• spinocerebellar ataxia type 6
• spondylocostal dysostosis
• trichothiodystrophy
• Weill-Marchesani syndrome
• xeroderma pigmentosum