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Concept information

... > Clinical finding (finding) > disease > Genetic disease > Hereditary disease > Autosomal hereditary disorder > Recessive hereditary disorder, NOS > Neurodegeneration due to 3-hydroxyisobutyryl coenzyme A hydrolase deficiency (disorder)
... > Clinical finding (finding) > Head and neck finding > Head finding (finding) > Finding of brain > Disease of brain > Cerebral degeneration > Neurodegeneration due to 3-hydroxyisobutyryl coenzyme A hydrolase deficiency (disorder)
... > Clinical finding (finding) > disease > Disorder of body system > Disease of nervous system > Disease of the central nervous system > Disease of brain > Cerebral degeneration > Neurodegeneration due to 3-hydroxyisobutyryl coenzyme A hydrolase deficiency (disorder)
... > Clinical finding (finding) > disease > Disease of head > Disease of brain > Cerebral degeneration > Neurodegeneration due to 3-hydroxyisobutyryl coenzyme A hydrolase deficiency (disorder)
... > Clinical finding (finding) > Head and neck finding > Head finding (finding) > Disease of head > Disease of brain > Cerebral degeneration > Neurodegeneration due to 3-hydroxyisobutyryl coenzyme A hydrolase deficiency (disorder)
... > Clinical finding (finding) > disease > Degenerative disorder > Degenerative disease of the central nervous system > Cerebral degeneration > Neurodegeneration due to 3-hydroxyisobutyryl coenzyme A hydrolase deficiency (disorder)

Preferred term

Neurodegeneration due to 3-hydroxyisobutyryl coenzyme A hydrolase deficiency (disorder)  

Type

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

Associated morphology

URI

http://www.irandoc.acir/onto/irandoc/722488009

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