Chromosome 17 issues: Alexander disease Andersen-Tawil syndrome Birt-Hogg-Dubé syndrome Bladder cancer Breast cancer Camptomelic dysplasia Canavan disease Cerebroretinal microangiopathy with calcifications and cysts Charcot-Marie-Tooth disease Charcot-Marie-Tooth disease, type 1 Corticobasal degeneration Cystinosis Depression Ehlers-Danlos syndrome Ehlers-Danlos syndrome, classical type Epidermodysplasia verruciformis Galactosemia Glycogen storage disease type II (Pompe disease) Hereditary neuropathy with liability to pressure palsies Howel–Evans syndrome Li-Fraumeni syndrome Maturity onset diabetes of the young type 5 Miller-Dieker syndrome Multiple synostoses syndrome Neurofibromatosis type I Nonsyndromic deafness Nonsyndromic deafness, autosomal dominant Nonsyndromic deafness, autosomal recessive Osteogenesis imperfecta Osteogenesis Imperfecta, Type I Osteogenesis Imperfecta, Type II Osteogenesis Imperfecta, Type III Osteogenesis Imperfecta, Type IV Potocki-Lupski syndrome Proximal symphalangism Smith-Magenis syndrome Usher syndrome Very long-chain acyl-coenzyme A dehydrogenase deficiency
Answered 5/20/2019
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A doctor has provided 1 answer
A doctor has provided 1 answer
A doctor has provided 1 answer
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