Conditions related to genes on chromosome 6

Genetics Home Reference includes these conditions related to genes on chromosome 6:

• age-related macular degeneration
• amyotrophic lateral sclerosis
• ankylosing spondylitis
• arginase deficiency
• autosomal recessive cerebellar ataxia type 1
• Axenfeld-Rieger syndrome
• Behçet disease
• branchio-oculo-facial syndrome
• Carpenter syndrome
• celiac disease
• Charcot-Marie-Tooth disease
• Char syndrome
• chordoma
• cleidocranial dysplasia
• Coffin-Siris syndrome
• congenital plasminogen deficiency
• critical congenital heart disease
• Dandy-Walker syndrome
• Diamond-Blackfan anemia
• Ehlers-Danlos syndrome
• hemochromatosis
• Huntington disease-like syndrome
• 21-hydroxylase deficiency
• hypermethioninemia
• idiopathic inflammatory myopathy
• juvenile idiopathic arthritis
• juvenile myoclonic epilepsy
• Lafora progressive myoclonus epilepsy
• 3-M syndrome
• maple syrup urine disease
• methylmalonic acidemia
• multiple epiphyseal dysplasia
• multiple sclerosis
• narcolepsy
• nonsyndromic deafness
• oculodentodigital dysplasia
• otospondylomegaepiphyseal dysplasia
• Parkinson disease
• polycystic kidney disease
• polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy
• pontocerebellar hypoplasia
• porphyria
• progressive pseudorheumatoid dysplasia
• psoriatic arthritis
• Refsum disease
• 6q24-related transient neonatal diabetes mellitus
• retinitis pigmentosa
• rhizomelic chondrodysplasia punctata
• sialic acid storage disease
• sialidosis
• spinocerebellar ataxia type 1
• Stargardt macular degeneration
• Stickler syndrome
• succinic semialdehyde dehydrogenase deficiency
• Treacher Collins syndrome
• trichothiodystrophy
• type 1 diabetes
• vitelliform macular dystrophy
• Weissenbacher-Zweymüller syndrome
• xeroderma pigmentosum
• X-linked sideroblastic anemia