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Concept information

... > Clinical finding (finding) > disease > Genetic disease > Hereditary disease > Autosomal hereditary disorder > Dominant hereditary disorder, NOS > Muscular atrophy, ataxia, retinitis pigmentosa, and diabetes mellitus
... > Clinical finding (finding) > disease > Disorder of muscle > Disorder of muscle > Amyotrophia > Muscular atrophy, ataxia, retinitis pigmentosa, and diabetes mellitus
... > Clinical finding (finding) > Muscular finding > Disorder of muscle > Disorder of muscle > Amyotrophia > Muscular atrophy, ataxia, retinitis pigmentosa, and diabetes mellitus
... > Clinical finding (finding) > Musculoskeletal system finding > Disease of the musculoskeletal system, NOS > Disorder of muscle > Amyotrophia > Muscular atrophy, ataxia, retinitis pigmentosa, and diabetes mellitus
... > Clinical finding (finding) > disease > Disorder of body system > Disease of the musculoskeletal system, NOS > Disorder of muscle > Amyotrophia > Muscular atrophy, ataxia, retinitis pigmentosa, and diabetes mellitus
... > Clinical finding (finding) > disease > Disorder of soft tissue > Disorder of muscle > Amyotrophia > Muscular atrophy, ataxia, retinitis pigmentosa, and diabetes mellitus
... > Clinical finding (finding) > General finding of soft tissue > Disorder of soft tissue > Disorder of muscle > Amyotrophia > Muscular atrophy, ataxia, retinitis pigmentosa, and diabetes mellitus
... > Clinical finding (finding) > Eye finding > Eyeball observation > Retina finding (finding) > Retinal disorder > Degeneration of retina > Muscular atrophy, ataxia, retinitis pigmentosa, and diabetes mellitus
... > Clinical finding (finding) > disease > Degenerative disorder > Degenerative disorder of globe > Degeneration of retina > Muscular atrophy, ataxia, retinitis pigmentosa, and diabetes mellitus

Preferred term

Muscular atrophy, ataxia, retinitis pigmentosa, and diabetes mellitus  

Type

  • http://www.irandoc.ac.ir/onto/irandoc-meta/Concept

Associated morphology

Associated with

URI

http://www.irandoc.acir/onto/irandoc/237611007

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