Human Phenotype Ontology 
Grandparent Node:
Abnormal nervous system physiology (HP:0012638)help
Parent Node:
Abnormal central sensory function (HP:0011730)help
..Starting node
Impaired touch localization (HP:0011811)help
Term ID: 11811
Name: Impaired touch localization
Synonym: Impaired topognosis; Impaired touch localisation
Definition: A reduced ability to identify precisely the site of a touch. This test is usually carried out by asking a patient, whose eyes are closed or covered, to touch the same site with a fingertip.
Reference: HP:0011811
Genes and Diseases:
       Child Nodes:

 Sister Nodes: 
..expandAgraphesthesia (HP:0011812) help
..expandAstereognosia (HP:0010527) help
..expandImpaired two-point discrimination (HP:0011810) help
InputHPO IDHPO termDistanceGeneGene id entrezDiseaseIdDiseaseNameDiseaseMIMConceptIDSourceTypical associationHGMD variantsClinVar variantsHGNC IDGeneMIM
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0011811HP:0011811Impaired touch localization0 CL E G H

Genes (0) :

Diseases (0) :

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