Conditions related to genes on chromosome 9

Genetics Home Reference includes these conditions related to genes on chromosome 9:

• amyotrophic lateral sclerosis
• ataxia with oculomotor apraxia
• benign essential blepharospasm
• Berardinelli-Seip congenital lipodystrophy
• 17-beta hydroxysteroid dehydrogenase 3 deficiency
• bladder cancer
• cap myopathy
• cartilage-hair hypoplasia
• chorea-acanthocytosis
• citrullinemia
• cytochrome c oxidase deficiency
• distal arthrogryposis type 1
• dopamine beta-hydroxylase deficiency
• early-onset primary dystonia
• Ehlers-Danlos syndrome
• essential thrombocythemia
• familial dysautonomia
• familial HDL deficiency
• familial thoracic aortic aneurysm and dissection
• Fanconi anemia
• Friedreich ataxia
• Fukuyama congenital muscular dystrophy
• galactosemia
• geleophysic dysplasia
• glycine encephalopathy
• Gorlin syndrome
• hereditary fructose intolerance
• hereditary hemorrhagic telangiectasia
• hereditary sensory neuropathy type 1
• inclusion body myopathy 2
• inclusion body myopathy with early-onset Paget disease and frontotemporal dementia
• Kleefstra syndrome
• lattice corneal dystrophy type II
• Leigh syndrome
• limb-girdle muscular dystrophy
• Loeys-Dietz syndrome
• lymphangioleiomyomatosis
• Manitoba oculotrichoanal syndrome
• 3-methylglutaconic aciduria
• 9q22.3 microdeletion
• multiple cutaneous and mucosal venous malformations
• nail-patella syndrome
• nemaline myopathy
• nonsyndromic deafness
• nonsyndromic holoprosencephaly
• oculocutaneous albinism
• polycythemia vera
• porphyria
• primary ciliary dyskinesia
• primary hyperoxaluria
• primary myelofibrosis
• Robinow syndrome
• sialuria
• Swyer syndrome
• Tangier disease
• thrombotic thrombocytopenic purpura
• tuberous sclerosis complex
• VLDLR-associated cerebellar hypoplasia
• xeroderma pigmentosum