Human Gene Set: HP_SUBCORTICAL_CEREBRAL_ATROPHY


Standard name HP_SUBCORTICAL_CEREBRAL_ATROPHY
Systematic name M38030
Brief description Subcortical cerebral atrophy
Full description or abstract Atrophy of the cerebral subcortical white and gray matter, termed subcortical atrophy, reflects loss of nerve cells in the basal ganglia or fibers in the deep white matter. [https://orcid.org/0000-0002-0736-9199, PMID:20813998]
Collection C5: Ontology
      HPO: Human Phenotype Ontology
Source publication  
Exact source HP:0012157
Related gene sets  
External links https://hpo.jax.org/app/browse/term/HP:0012157
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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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Version history 2024.1.Hs: Updated to HPO Release 2024-04-26.

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