Biological Sciences and Healthcare, part 4

... > 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 > Hereditary degenerative disease of central nervous system > Hereditary cerebellar degeneration > Spinocerebellar ataxia > Autosomal recessive cerebellar ataxia-epilepsy-intellectual disability syndrome due to RUBCN (RUN and cysteine rich domain containing beclin 1 interacting protein) deficiency

... > Clinical finding (finding) > disease > Degenerative disorder > Degenerative disease of the central nervous system > Hereditary degenerative disease of central nervous system > Hereditary cerebellar degeneration > Spinocerebellar ataxia > Autosomal recessive cerebellar ataxia-epilepsy-intellectual disability syndrome due to RUBCN (RUN and cysteine rich domain containing beclin 1 interacting protein) deficiency

... > Clinical finding (finding) > Head and neck finding > Head finding (finding) > Finding of brain > Disease of brain > Cerebral degeneration > Cerebellar degeneration > Hereditary cerebellar degeneration > Spinocerebellar ataxia > Autosomal recessive cerebellar ataxia-epilepsy-intellectual disability syndrome due to RUBCN (RUN and cysteine rich domain containing beclin 1 interacting protein) 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 > Spinocerebellar ataxia > Autosomal recessive cerebellar ataxia-epilepsy-intellectual disability syndrome due to RUBCN (RUN and cysteine rich domain containing beclin 1 interacting protein) deficiency

... > Clinical finding (finding) > disease > Disease of head > Disease of brain > Cerebral degeneration > Cerebellar degeneration > Hereditary cerebellar degeneration > Spinocerebellar ataxia > Autosomal recessive cerebellar ataxia-epilepsy-intellectual disability syndrome due to RUBCN (RUN and cysteine rich domain containing beclin 1 interacting protein) deficiency

... > Clinical finding (finding) > Head and neck finding > Head finding (finding) > Disease of head > Disease of brain > Cerebral degeneration > Cerebellar degeneration > Hereditary cerebellar degeneration > Spinocerebellar ataxia > Autosomal recessive cerebellar ataxia-epilepsy-intellectual disability syndrome due to RUBCN (RUN and cysteine rich domain containing beclin 1 interacting protein) 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 > Spinocerebellar ataxia > Autosomal recessive cerebellar ataxia-epilepsy-intellectual disability syndrome due to RUBCN (RUN and cysteine rich domain containing beclin 1 interacting protein) deficiency

... > Clinical finding (finding) > disease > Degenerative disorder > Degenerative disease of the central nervous system > Cerebral degeneration > Cerebellar degeneration > Hereditary cerebellar degeneration > Spinocerebellar ataxia > Autosomal recessive cerebellar ataxia-epilepsy-intellectual disability syndrome due to RUBCN (RUN and cysteine rich domain containing beclin 1 interacting protein) deficiency

... > Clinical finding (finding) > Finding of coordination > Ataxia > Hereditary ataxia (disorder) > Spinocerebellar ataxia > Autosomal recessive cerebellar ataxia-epilepsy-intellectual disability syndrome due to RUBCN (RUN and cysteine rich domain containing beclin 1 interacting protein) 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 RUBCN (RUN and cysteine rich domain containing beclin 1 interacting protein) deficiency