Human Phenotype Ontology 
Grandparent Node:
expandAbnormality of the cerebral subcortex (HP:0010993)help
Parent Node:
expandAbnormality of the basal ganglia (HP:0002134)help
..Starting node
..expandSymmetric lesions of the basal ganglia (HP:0007039)help
Term ID: 7039
Name: Symmetric lesions of the basal ganglia
Synonym:
Definition:
Comments:
Reference: HP:0007039
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandAbnormal basal ganglia MRI signal intensity (HP:0012751) help
..expandAbnormal corpus striatum morphology (HP:0010994) help
..expandAbnormal globus pallidus morphology (HP:0002453) help
..expandAbnormal substantia nigra morphology (HP:0045007) help
..expandBasal ganglia calcification (HP:0002135) help
..expandBasal ganglia cysts (HP:0006799) help
..expandBasal ganglia edema (HP:0025039) help
..expandBasal ganglia gliosis (HP:0006999) help
..expandBasal ganglia necrosis (HP:0012128) help
..expandBilateral basal ganglia lesions (HP:0007146) help
..expandCavitation of the basal ganglia (HP:0007007) help
..expandDysgenesis of the basal ganglia (HP:0025102) help
..expandHemiballismus (HP:0100248) help
..expandLarge basal ganglia (HP:0007048) help
..expandNeuronal loss in basal ganglia (HP:0200147) help
..expandSmall basal ganglia (HP:0012697) help
..expandStatus cribrosum (HP:0025012) help
InputHPO IDHPO termDistanceGeneGene id entrezDiseaseIdDiseaseNameDiseaseMIMConceptIDSourceTypical associationHGMD variantsClinVar variantsHGNC IDGeneMIM
 
HPO disease - gene - phenotype typical associations:
HP:0007039HP:0007039Symmetric lesions of the basal ganglia0PDE8B CL E G H8622609161Striatal degeneration, autosomal dominant 1609161C4310808OMIM12438794603390
 
HPO disease - gene - phenotype less frequent non-typical associations:


Genes (1) :PDE8B

Diseases (1) :609161
 

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