Conditions related to genes on chromosome 12

Genetics Home Reference includes these conditions related to genes on chromosome 12:

• achondrogenesis
• amyotrophic lateral sclerosis
• Czech dysplasia
• Darier disease
• dentatorubral-pallidoluysian atrophy
• epidermolysis bullosa simplex
• episodic ataxia
• hereditary hemorrhagic telangiectasia
• Holt-Oram syndrome
• hypochondrogenesis
• Kniest dysplasia
• leukoencephalopathy with vanishing white matter
• methylmalonic acidemia
• nonsyndromic deafness
• Noonan syndrome
• pachyonychia congenita
• Parkinson disease
• phenylketonuria
• platyspondylic lethal skeletal dysplasia, Torrance type
• short-chain acyl-coenzyme A dehydrogenase deficiency
• spondyloepimetaphyseal dysplasia, Strudwick type
• spondyloepiphyseal dysplasia congenita
• spondyloperipheral dysplasia
• Stickler syndrome
• Swyer syndrome
• Timothy syndrome
• tyrosinemia
• von Willebrand disease

GeneCards provides a table of genes on chromosome 12 and disorders related to those genes.