Conditions related to genes on chromosome 7

Genetics Home Reference includes these conditions related to genes on chromosome 7:

• argininosuccinic aciduria
• aromatic l-amino acid decarboxylase deficiency
• Baraitser-Winter syndrome
• cardiofaciocutaneous syndrome
• cerebral cavernous malformation
• Charcot-Marie-Tooth disease
• chronic granulomatous disease
• citrullinemia
• coloboma
• color vision deficiency
• congenital bilateral absence of the vas deferens
• cutis laxa
• cystic fibrosis
• cytochrome P450 oxidoreductase deficiency
• distal hereditary motor neuropathy, type II
• distal hereditary motor neuropathy, type V
• Ehlers-Danlos syndrome
• familial hypertrophic cardiomyopathy
• Greig cephalopolysyndactyly syndrome
• hand-foot-genital syndrome
• hemochromatosis
• hereditary pancreatitis
• hyperlysinemia
• hypomyelination and congenital cataract
• intrahepatic cholestasis of pregnancy
• isolated growth hormone deficiency
• Langerhans cell histiocytosis
• Lynch syndrome
• maple syrup urine disease
• microphthalmia
• mucopolysaccharidosis type VII
• multiple lentigines syndrome
• myoclonus-dystonia
• myotonia congenita
• nonsyndromic deafness
• nonsyndromic holoprosencephaly
• Noonan syndrome
• osteogenesis imperfecta
• Pallister-Hall syndrome
• Pendred syndrome
• phosphoglycerate mutase deficiency
• progressive familial intrahepatic cholestasis
• pyruvate dehydrogenase deficiency
• Romano-Ward syndrome
• Saethre-Chotzen syndrome
• short QT syndrome
• Shwachman-Diamond syndrome
• spondylocostal dysostosis
• supravalvular aortic stenosis
• systemic scleroderma
• trichothiodystrophy
• Williams syndrome
• Wolff-Parkinson-White syndrome
• Zellweger spectrum