Conditions related to genes on chromosome 11

Genetics Home Reference includes these conditions related to genes on chromosome 11:

• age-related macular degeneration
• Aicardi-Goutieres syndrome
• amelogenesis imperfecta
• aniridia
• ataxia-telangiectasia
• Bardet-Biedl syndrome
• Bartter syndrome
• Beckwith-Wiedemann syndrome
• Berardinelli-Seip congenital lipodystrophy
• beta-ketothiolase deficiency
• beta thalassemia
• bladder cancer
• breast cancer
• carnitine palmitoyltransferase I deficiency
• CATSPER1-related nonsyndromic male infertility
• Charcot-Marie-Tooth disease
• coloboma
• congenital fibrosis of the extraocular muscles
• congenital myasthenic syndrome
• Costello syndrome
• cutis laxa
• distal hereditary motor neuropathy, type V
• dopa-responsive dystonia
• enlarged parietal foramina
• familial atrial fibrillation
• familial exudative vitreoretinopathy
• familial hyperinsulinism
• familial Mediterranean fever
• glycogen storage disease type I
• glycogen storage disease type V
• hereditary angioedema
• hereditary multiple exostoses
• hereditary paraganglioma-pheochromocytoma
• horizontal gaze palsy with progressive scoliosis
• isobutyryl-CoA dehydrogenase deficiency
• Jervell and Lange-Nielsen syndrome
• lactate dehydrogenase deficiency
• limb-girdle muscular dystrophy
• methemoglobinemia, beta-globin type
• microphthalmia
• multiple endocrine neoplasia
• multiple pterygium syndrome
• neutral lipid storage disease with myopathy
• Niemann-Pick disease
• nonsyndromic deafness
• nonsyndromic paraganglioma
• oculocutaneous albinism
• osteopetrosis
• permanent neonatal diabetes mellitus
• porphyria
• prothrombin deficiency
• prothrombin thrombophilia
• pyruvate carboxylase deficiency
• retinitis pigmentosa
• Romano-Ward syndrome
• Russell-Silver syndrome
• short QT syndrome
• sickle cell disease
• Silver syndrome
• Smith-Lemli-Opitz syndrome
• spinal muscular atrophy
• tetrahydrobiopterin deficiency
• tyrosine hydroxylase deficiency
• Usher syndrome
• vitelliform macular dystrophy
• Wilms tumor, aniridia, genitourinary anomalies, and mental retardation syndrome