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... > Clinical finding (finding) > disease > Degenerative disorder > Degenerative disease of the central nervous system > Hereditary degenerative disease of central nervous system > Hereditary cerebellar degeneration > Autosomal recessive cerebellar ataxia, epilepsy, intellectual disability syndrome due to WWOX (WW domain containing oxidoreductase) deficiency
... > Clinical finding (finding) > Head and neck finding > Head finding (finding) > Finding of brain > Disease of brain > Cerebral degeneration > Cerebellar degeneration > Hereditary cerebellar degeneration > Autosomal recessive cerebellar ataxia, epilepsy, intellectual disability syndrome due to WWOX (WW domain containing oxidoreductase) deficiency
... > Clinical finding (finding) > disease > Disorder of body system > Disease of nervous system > Disease of the central nervous system > Disease of brain > Cerebral degeneration > Cerebellar degeneration > Hereditary cerebellar degeneration > Autosomal recessive cerebellar ataxia, epilepsy, intellectual disability syndrome due to WWOX (WW domain containing oxidoreductase) deficiency
... > Clinical finding (finding) > disease > Disease of head > Disease of brain > Cerebral degeneration > Cerebellar degeneration > Hereditary cerebellar degeneration > Autosomal recessive cerebellar ataxia, epilepsy, intellectual disability syndrome due to WWOX (WW domain containing oxidoreductase) deficiency
... > Clinical finding (finding) > Head and neck finding > Head finding (finding) > Disease of head > Disease of brain > Cerebral degeneration > Cerebellar degeneration > Hereditary cerebellar degeneration > Autosomal recessive cerebellar ataxia, epilepsy, intellectual disability syndrome due to WWOX (WW domain containing oxidoreductase) deficiency
... > Clinical finding (finding) > disease > Disorder of body system > Disease of nervous system > Disease of the central nervous system > Degenerative disease of the central nervous system > Cerebral degeneration > Cerebellar degeneration > Hereditary cerebellar degeneration > Autosomal recessive cerebellar ataxia, epilepsy, intellectual disability syndrome due to WWOX (WW domain containing oxidoreductase) deficiency
... > Clinical finding (finding) > disease > Degenerative disorder > Degenerative disease of the central nervous system > Cerebral degeneration > Cerebellar degeneration > Hereditary cerebellar degeneration > Autosomal recessive cerebellar ataxia, epilepsy, intellectual disability syndrome due to WWOX (WW domain containing oxidoreductase) deficiency
... > Clinical finding (finding) > disease > Genetic disease > Hereditary disease > Autosomal hereditary disorder > Recessive hereditary disorder, NOS > Autosomal recessive cerebellar ataxia, epilepsy, intellectual disability syndrome due to WWOX (WW domain containing oxidoreductase) deficiency
... > Clinical finding (finding) > disease > mental disorder > Developmental mental disorder > Intellectual disability > Autosomal recessive cerebellar ataxia, epilepsy, intellectual disability syndrome due to WWOX (WW domain containing oxidoreductase) deficiency
... > Clinical finding (finding) > disease > developmental disorder > Neurodevelopmental disorder > Developmental mental disorder > Intellectual disability > Autosomal recessive cerebellar ataxia, epilepsy, intellectual disability syndrome due to WWOX (WW domain containing oxidoreductase) deficiency
Clinical finding (finding) > Finding of coordination > Ataxia > Hereditary ataxia (disorder) > Autosomal recessive cerebellar ataxia, epilepsy, intellectual disability syndrome due to WWOX (WW domain containing oxidoreductase) deficiency

Preferred term

Autosomal recessive cerebellar ataxia, epilepsy, intellectual disability syndrome due to WWOX (WW domain containing oxidoreductase) deficiency  

Type

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

Associated morphology

URI

http://www.irandoc.acir/onto/irandoc/770898002

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