Human Phenotype Ontology 
Grandparent Node:
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Abnormality of the basal ganglia (HP:0002134)help
Parent Node:
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Abnormal basal ganglia MRI signal intensity (HP:0012751)help
..Starting node
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Focal T2 hypointense basal ganglia lesion (HP:0012752)help
Term ID: 12752
Name: Focal T2 hypointense basal ganglia lesion
Synonym:
Definition: A darker than expected T2 signal on magnetic resonance imaging (MRI) of the basal ganglia. This term refers to a localized hypointensity affecting a particular region of the basal ganglia.
Comments:
Reference: HP:0012752
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandFocal T2 hyperintense basal ganglia lesion (HP:0007183) help
..expandT2 hypointense basal ganglia (HP:0012753) help
InputHPO IDHPO termDistanceGeneGene id entrezDiseaseIdDiseaseNameDiseaseMIMConceptIDSourceTypical associationHGMD variantsClinVar variantsHGNC IDGeneMIM
 
HPO disease - gene - phenotype typical associations:
HP:0012752HP:0012752Focal T2 hypointense basal ganglia lesion0COQ8A CL E G H56997139485ORPHA169916812606980
 
HPO disease - gene - phenotype less frequent non-typical associations:


Genes (1) :COQ8A

Diseases (1) :139485
 

Human Phenotype Ontology(HPO) is developed by the Human Phenotype Ontology Consortium. The version used here is August 2021 release.