Conditions related to genes on chromosome 8

Genetics Home Reference includes these conditions related to genes on chromosome 8:

• ataxia with vitamin E deficiency
• autosomal dominant nocturnal frontal lobe epilepsy
• Baller-Gerold syndrome
• benign familial neonatal seizures
• branchiootorenal syndrome
• breast cancer
• Charcot-Marie-Tooth disease
• CHARGE syndrome
• Cohen syndrome
• coloboma
• color vision deficiency
• congenital adrenal hyperplasia due to 11-beta-hydroxylase deficiency
• congenital hypothyroidism
• congenital myasthenic syndrome
• epidermolysis bullosa simplex
• epidermolysis bullosa with pyloric atresia
• familial hyperaldosteronism
• familial idiopathic basal ganglia calcification
• familial lipoprotein lipase deficiency
• Farber lipogranulomatosis
• hereditary multiple exostoses
• hereditary spherocytosis
• idiopathic pulmonary fibrosis
• juvenile Paget disease
• Kallmann syndrome
• Klippel-Feil syndrome
• Langer-Giedion syndrome
• microphthalmia
• mucopolysaccharidosis type III
• Nijmegen breakage syndrome
• Paget disease of bone
• Pfeiffer syndrome
• piebaldism
• pyruvate dehydrogenase deficiency
• Roberts syndrome
• Rothmund-Thomson Syndrome
• spastic paraplegia type 8
• surfactant dysfunction
• Waardenburg syndrome
• Werner syndrome