Conditions related to genes on chromosome 17

Genetics Home Reference includes these conditions related to genes on chromosome 17:

• acute promyelocytic leukemia
• Alexander disease
• Amish lethal microcephaly
• Andersen-Tawil syndrome
• Birt-Hogg-Dubé syndrome
• bladder cancer
• breast cancer
• campomelic dysplasia
• Canavan disease
• Carney complex
• Charcot-Marie-Tooth disease
• common variable immune deficiency
• congenital myasthenic syndrome
• cystinosis
• dermatofibrosarcoma protuberans
• Ehlers-Danlos syndrome
• epidermolysis bullosa simplex
• epidermolysis bullosa with pyloric atresia
• epidermolytic hyperkeratosis
• familial atrial fibrillation
• familial hemophagocytic lymphohistiocytosis
• Fanconi anemia
• Freeman-Sheldon syndrome
• frontotemporal dementia with parkinsonism-17
• galactosemia
• glycogen storage disease type I
• GRN-related frontotemporal dementia
• hereditary folate malabsorption
• hereditary neuralgic amyotrophy
• hereditary neuropathy with liability to pressure palsies
• hyperkalemic periodic paralysis
• hypokalemic periodic paralysis
• isolated growth hormone deficiency
• Job syndrome
• Leber congenital amaurosis
• Li-Fraumeni syndrome
• limb-girdle muscular dystrophy
• Miller-Dieker syndrome
• mucopolysaccharidosis type III
• N-acetylglutamate synthase deficiency
• neuroblastoma
• neurofibromatosis type 1
• nonbullous congenital ichthyosiform erythroderma
• nonsyndromic deafness
• osteogenesis imperfecta
• pachyonychia congenita
• paramyotonia congenita
• Pompe disease
• pontocerebellar hypoplasia
• potassium-aggravated myotonia
• progressive supranuclear palsy
• pseudohypoaldosteronism type 2
• pyridoxal 5'-phosphate-dependent epilepsy
• short QT syndrome
• Sjögren-Larsson syndrome
• Smith-Magenis syndrome
• SOST-related sclerosing bone dysplasia
• spondylocostal dysostosis
• tarsal-carpal coalition syndrome
• tetra-amelia syndrome
• Usher syndrome
• very long-chain acyl-CoA dehydrogenase deficiency
• vitiligo