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Accession:DOID:9007548 term browser browse the term
Definition:A recessively inherited neurodegenerative disorder that affects the white matter of the central nervous system (CNS). (
Synonyms:exact_synonym: LEMP
 primary_id: OMIA:001788
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  disease 16017
    disease of anatomical entity 15273
      nervous system disease 10762
        neurodegenerative disease 3140
          Nervous System Heredodegenerative Disorders 1898
            Leukoencephalomyelopathy 0
Path 2
Term Annotations click to browse term
  disease 16017
    Developmental Diseases 9307
      Congenital, Hereditary, and Neonatal Diseases and Abnormalities 8132
        genetic disease 7652
          monogenic disease 5403
            autosomal genetic disease 4361
              autosomal recessive disease 2342
                Leukoencephalomyelopathy 0
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RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.