Human Phenotype Ontology 
Grandparent Node:
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Abnormality of movement (HP:0100022)help
Parent Node:
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Dyskinesia (HP:0100660)help
..Starting node
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Tardive dyskinesia (HP:0040141)help
Term ID: 40141
Name: Tardive dyskinesia
Synonym:
Definition:
Comments:
Reference: HP:0040141
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandExtrapyramidal dyskinesia (HP:0007308) help
..expandOrofacial dyskinesia (HP:0002310) 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:0040141HP:0040141Tardive dyskinesia0 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.