Human Gene Set: HP_FOCAL_T2_HYPERINTENSE_BASAL_GANGLIA_LESION


Standard name HP_FOCAL_T2_HYPERINTENSE_BASAL_GANGLIA_LESION
Systematic name M41351
Brief description Focal T2 hyperintense basal ganglia lesion
Full description or abstract A lighter than expected T2 signal on magnetic resonance imaging (MRI) of the basal ganglia. This term refers to a localized hyperintensity affecting a particular region of the basal ganglia. [https://orcid.org/0000-0002-0736-9199]
Collection C5: Ontology
      HPO: Human Phenotype Ontology
Source publication  
Exact source HP:0007183
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External links https://hpo.jax.org/app/browse/term/HP:0007183
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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
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Version history 2025.1.Hs: Updated to HPO Release 2025-05-06.

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