skip to main content

Content language

Contact us: CRM@email.irandoc.ac.ir

Concept information

... > Clinical finding (finding) > disease > Genetic disease > Hereditary disease > Autosomal hereditary disorder > Dominant hereditary disorder, NOS > Hypomyelinating leukodystrophy with atrophy of basal ganglia and cerebellum (disorder)
... > Clinical finding (finding) > disease > Disease of head > Disease of brain > Cerebral degeneration > Cerebral degeneration (disorder) > Cerebral atrophy > Hypomyelinating leukodystrophy with atrophy of basal ganglia and cerebellum (disorder)
... > Clinical finding (finding) > Head and neck finding > Head finding (finding) > Disease of head > Disease of brain > Cerebral degeneration > Cerebral degeneration (disorder) > Cerebral atrophy > Hypomyelinating leukodystrophy with atrophy of basal ganglia and cerebellum (disorder)
Clinical finding (finding) > Finding of coordination > Ataxia > Hereditary ataxia (disorder) > Hypomyelinating leukodystrophy with atrophy of basal ganglia and cerebellum (disorder)
... > Clinical finding (finding) > disease > Disorder of body system > Disease of nervous system > Neuropathy (disorder) > Leucodystrophy > TUBB4A-related leukodystrophy > Hypomyelinating leukodystrophy with atrophy of basal ganglia and cerebellum (disorder)
... > Clinical finding (finding) > disease > Degenerative disorder > Degenerative disease of the central nervous system > Leucodystrophy > TUBB4A-related leukodystrophy > Hypomyelinating leukodystrophy with atrophy of basal ganglia and cerebellum (disorder)

Preferred term

Hypomyelinating leukodystrophy with atrophy of basal ganglia and cerebellum (disorder)  

Type

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

Associated morphology

Finding site

URI

http://www.irandoc.acir/onto/irandoc/724283004

Download this concept: