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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GTEx compendium
Human tissue compendium (Novartis)
Global Cancer Map (Broad Institute)
NCI-60 cell lines (National Cancer Institute)
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Show members (show 222 source identifiers mapped to 222 genes)
Version history 2023.1.Hs: Updated to HPO Release 2023-01-27.

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