Human Phenotype Ontology 
Grandparent Node:
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Mental deterioration (HP:0001268)help
Parent Node:
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Dementia (HP:0000726)help
..Starting node
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Frontolimbic dementia (HP:0002439)help
Term ID: 2439
Name: Frontolimbic dementia
Synonym:
Definition:
Comments:
Reference: HP:0002439
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandFrontal lobe dementia (HP:0000727) help
..expandFrontotemporal dementia (HP:0002145) help
..expandSubcortical dementia (HP:0007123) help
InputHPO IDHPO termDistanceGeneGene id entrezDiseaseIdDiseaseNameDiseaseMIMConceptIDSourceTypical associationHGMD variantsClinVar variantsHGNC IDGeneMIM
 
HPO disease - gene - phenotype typical associations:
HP:0002439HP:0002439Frontolimbic dementia0MAPT CL E G H4137601104Progressive supranuclear ophthalmoplegia601104C0038868OMIM15816893157140
 
HPO disease - gene - phenotype less frequent non-typical associations:


Genes (1) :MAPT

Diseases (1) :601104
 

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