Conditions related to genes on chromosome 10

Genetics Home Reference includes these conditions related to genes on chromosome 10:

• age-related macular degeneration
• Apert syndrome
• ataxia neuropathy spectrum
• autoimmune lymphoproliferative syndrome
• autosomal dominant partial epilepsy with auditory features
• Bannayan-Riley-Ruvalcaba syndrome
• Beare-Stevenson cutis gyrata syndrome
• cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy
• Charcot-Marie-Tooth disease
• cholesteryl ester storage disease
• CHST3-related skeletal dysplasia
• Cockayne syndrome
• congenital myasthenic syndrome
• Cornelia de Lange syndrome
• Cowden syndrome
• Crouzon syndrome
• Diamond-Blackfan anemia
• Dubin-Johnson syndrome
• familial hemophagocytic lymphohistiocytosis
• familial thoracic aortic aneurysm and dissection
• genitopatellar syndrome
• gyrate atrophy of the choroid and retina
• Hermansky-Pudlak syndrome
• Hirschsprung disease
• hypermethioninemia
• infantile-onset spinocerebellar ataxia
• Jackson-Weiss syndrome
• junctional epidermolysis bullosa
• juvenile polyposis syndrome
• mannose-binding lectin deficiency
• metachromatic leukodystrophy
• 2-methylbutyryl-CoA dehydrogenase deficiency
• multiple endocrine neoplasia
• myofibrillar myopathy
• nonsyndromic deafness
• nonsyndromic paraganglioma
• Ochoa syndrome
• Ohdo syndrome, Say-Barber-Biesecker-Young-Simpson variant
• Pfeiffer syndrome
• porphyria
• progressive external ophthalmoplegia
• Refsum disease
• renal coloboma syndrome
• tetrahydrobiopterin deficiency
• Usher syndrome
• UV-sensitive syndrome
• Wolman disease