Conditions related to genes on chromosome 5

Genetics Home Reference includes these conditions related to genes on chromosome 5:

• achondrogenesis
• amyotrophic lateral sclerosis
• ankylosing spondylitis
• atelosteogenesis type 2
• breast cancer
• capillary malformation-arteriovenous malformation syndrome
• Charcot-Marie-Tooth disease
• chylomicron retention disease
• Cockayne syndrome
• combined pituitary hormone deficiency
• congenital contractural arachnodactyly
• Cornelia de Lange syndrome
• craniometaphyseal dysplasia
• cri-du-chat syndrome
• Crohn disease
• diastrophic dysplasia
• distal myopathy 2
• dyskeratosis congenita
• Ehlers-Danlos syndrome
• enlarged parietal foramina
• episodic ataxia
• familial adenomatous polyposis
• GM2-gangliosidosis, AB variant
• hereditary angioedema
• hereditary hyperekplexia
• hereditary sensory and autonomic neuropathy type II
• homocystinuria
• idiopathic pulmonary fibrosis
• lattice corneal dystrophy type I
• Leigh syndrome
• limb-girdle muscular dystrophy
• Marinesco-Sjögren syndrome
• 3-methylcrotonyl-CoA carboxylase deficiency
• Milroy disease
• mucopolysaccharidosis type VI
• multiple epiphyseal dysplasia
• myofibrillar myopathy
• nonsyndromic paraganglioma
• oculocutaneous albinism
• Paget disease of bone
• Parkes Weber syndrome
• primary carnitine deficiency
• primary ciliary dyskinesia
• pyridoxine-dependent epilepsy
• Sandhoff disease
• Sotos syndrome
• spinal muscular atrophy
• succinyl-CoA:3-ketoacid CoA transferase deficiency
• Treacher Collins syndrome
• Usher syndrome
• Wagner syndrome