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Human Disease

typical adult-onset autosomal dominant demyelinating leukodystrophy

Term ID
DOID:0060785
Synonyms
  • ADLD
  • adult-onset autosomal dominant leukodystrophy
  • autosomal-dominant or late-onset type Pelizaeus-Merzbacher disease
Definition
An adult onset demyelinating leukodystrophy characterized by autonomic abnormalities, pyramidal and cerebellar dysfunction, and symmetric demyelination of the CNS, presenting in the fourth or fifth decade of life, and that has_material_basis_in a heterozygous tandem genomic duplication on chromosome 5q23 that results in an extra copy of the lamin B1 gene (LMNB1), but also alters regulatory sequences that affect expression of other genes. (3)
References
  • GARD:10587
  • MIM:169500
  • SNOMEDCT_US_2023_03_01:448054001
  • UMLS_CUI:C3164344
Ontology
Human Disease   ( DOID:0060785 )
Relationships
is a type of
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Genes Involved
Zebrafish Models