Human Gene Set: HP_LEUKOENCEPHALOPATHY


Standard name HP_LEUKOENCEPHALOPATHY
Systematic name M35789
Brief description Leukoencephalopathy
Full description or abstract This term describes abnormality of the white matter of the cerebrum resulting from damage to the myelin sheaths of nerve cells. [https://orcid.org/0000-0002-0736-9199]
Collection C5: Ontology
      HPO: Human Phenotype Ontology
Source publication  
Exact source HP:0002352
Related gene sets  
External links https://hpo.jax.org/app/browse/term/HP:0002352
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Source species Homo sapiens
Contributed by Human Phenotype Ontology Group (The Jackson Laboratory (JAX))
Source platform or
identifier namespace		 Human_NCBI_Gene_ID
Dataset references  
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NCI-60 cell lines (National Cancer Institute)
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Version history 2026.1.Hs: Updated to HPO Release 2026-01-08.


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