Conditions related to genes on chromosome 2

Genetics Home Reference includes these conditions related to genes on chromosome 2:

• African iron overload
• 5-alpha reductase deficiency
• Alport syndrome
• Alström syndrome
• amyotrophic lateral sclerosis
• ankylosing spondylitis
• benign recurrent intrahepatic cholestasis
• Bethlem myopathy
• breast cancer
• carbamoyl phosphate synthetase I deficiency
• centronuclear myopathy
• cerebrotendinous xanthomatosis
• color vision deficiency
• congenital hypothyroidism
• congenital insensitivity to pain
• craniofacial-deafness-hand syndrome
• Crigler-Najjar syndrome
• Crohn disease
• cystinuria
• deoxyguanosine kinase deficiency
• Diamond-Blackfan anemia
• Donnai-Barrow syndrome
• dopa-responsive dystonia
• early-onset glaucoma
• Ehlers-Danlos syndrome
• epidermolysis bullosa with pyloric atresia
• episodic ataxia
• erythromelalgia
• essential tremor
• familial erythrocytosis
• familial hemiplegic migraine
• familial hypertrophic cardiomyopathy
• familial hypobetalipoproteinemia
• familial male-limited precocious puberty
• familial paroxysmal nonkinesigenic dyskinesia
• Feingold syndrome
• fibrodysplasia ossificans progressiva
• Gilbert syndrome
• harlequin ichthyosis
• hemochromatosis
• hepatic veno-occlusive disease with immunodeficiency
• hereditary myopathy with early respiratory failure
• homocystinuria
• 2-hydroxyglutaric aciduria
• hypercholesterolemia
• hyperphosphatemic familial tumoral calcinosis
• hypohidrotic ectodermal dysplasia
• idiopathic inflammatory myopathy
• infantile-onset ascending hereditary spastic paralysis
• intrahepatic cholestasis of pregnancy
• isolated Duane retraction syndrome
• juvenile idiopathic arthritis
• juvenile myoclonic epilepsy
• juvenile primary lateral sclerosis
• lactose intolerance
• lamellar ichthyosis
• leukoencephalopathy with vanishing white matter
• Leydig cell hypoplasia
• limb-girdle muscular dystrophy
• long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency
• Lynch syndrome
• methylmalonic acidemia
• mitochondrial trifunctional protein deficiency
• Mowat-Wilson syndrome
• MPV17-related hepatocerebral mitochondrial DNA depletion syndrome
• multiple epiphyseal dysplasia
• multiple pterygium syndrome
• myofibrillar myopathy
• myostatin-related muscle hypertrophy
• nemaline myopathy
• neuroblastoma
• nonsyndromic deafness
• nonsyndromic holoprosencephaly
• nonsyndromic paraganglioma
• Noonan syndrome
• paroxysmal extreme pain disorder
• Perry syndrome
• primary hyperoxaluria
• progressive familial intrahepatic cholestasis
• protein C deficiency
• pulmonary arterial hypertension
• rhizomelic chondrodysplasia punctata
• Salih myopathy
• Schimke immuno-osseous dysplasia
• sepiapterin reductase deficiency
• small fiber neuropathy
• spastic paraplegia type 4
• succinate-CoA ligase deficiency
• surfactant dysfunction
• systemic scleroderma
• tibial muscular dystrophy
• trichothiodystrophy
• Ullrich congenital muscular dystrophy
• Waardenburg syndrome
• xeroderma pigmentosum
• ZAP70-related severe combined immunodeficiency