Conditions related to genes on chromosome 4

Genetics Home Reference includes these conditions related to genes on chromosome 4:

• abetalipoproteinemia
• achondroplasia
• age-related macular degeneration
• amelogenesis imperfecta
• aspartylglucosaminuria
• atypical hemolytic-uremic syndrome
• Axenfeld-Rieger syndrome
• benign essential blepharospasm
• beta-mannosidosis
• Bietti crystalline dystrophy
• bladder cancer
• cherubism
• complement factor I deficiency
• congenital afibrinogenemia
• congenital central hypoventilation syndrome
• congenital myasthenic syndrome
• Crouzonodermoskeletal syndrome
• dentinogenesis imperfecta
• Ellis-van Creveld syndrome
• epidermal nevus
• essential thrombocythemia
• familial hyperinsulinism
• gastrointestinal stromal tumor
• glutaric acidemia type II
• Huntington disease
• 3-hydroxyacyl-CoA dehydrogenase deficiency
• hypochondroplasia
• infantile systemic hyalinosis
• juvenile hyaline fibromatosis
• limb-girdle muscular dystrophy
• methylmalonic acidemia
• mucopolysaccharidosis type I
• Muenke syndrome
• multiple system atrophy
• neuroblastoma
• nonsyndromic deafness
• Parkinson disease
• PDGFRA-associated chronic eosinophilic leukemia
• piebaldism
• polycystic kidney disease
• polycythemia vera
• primary myelofibrosis
• progressive external ophthalmoplegia
• pseudohypoaldosteronism type 1
• Romano-Ward syndrome
• SADDAN
• tetrahydrobiopterin deficiency
• thanatophoric dysplasia
• UV-sensitive syndrome
• Weyers acrofacial dysostosis
• Wolf-Hirschhorn syndrome
• Wolfram syndrome