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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Frontal lobe dementia (HP:0000727)help
Term ID: 727
Name: Frontal lobe dementia
Synonym:
Definition:
Comments:
Reference: HP:0000727
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandFrontolimbic dementia (HP:0002439) help
..expandFrontotemporal dementia (HP:0002145) help
..expandSubcortical dementia (HP:0007123) help
InputHPO IDHPO termDistanceGeneGene id entrezHGNC IDDiseaseIdDiseaseNameFrequencyOnsetHGMD variantsClinVar variants
 
HPO disease - gene - phenotype typical associations:
 
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0000727HP:0000727Frontal lobe dementia0CHCHD10 CL E G H40091615559OMIM:615911Frontotemporal dementia and/or amyotrophic lateral sclerosis 2.11
HP:0000727HP:0000727Frontal lobe dementia0CSF1R CL E G H14362433OMIM:221820Leukoencephalopathy, diffuse hereditary, with spheroids.149
HP:0000727HP:0000727Frontal lobe dementia0DNAJC6 CL E G H982915469ORPHA:2828Young-onset Parkinson diseaseHP:0040284 - Very rare6
HP:0000727HP:0000727Frontal lobe dementia0FTL CL E G H25123999ORPHA:157846NeuroferritinopathyHP:0040284 - Very rare33
HP:0000727HP:0000727Frontal lobe dementia0HTRA2 CL E G H2742914348ORPHA:2828Young-onset Parkinson diseaseHP:0040284 - Very rare39
HP:0000727HP:0000727Frontal lobe dementia0LRRK2 CL E G H12089218618ORPHA:2828Young-onset Parkinson diseaseHP:0040284 - Very rare221
HP:0000727HP:0000727Frontal lobe dementia0MAPT CL E G H41376893OMIM:600274Frontotemporal dementia.140
HP:0000727HP:0000727Frontal lobe dementia0PARK7 CL E G H1131516369ORPHA:2828Young-onset Parkinson diseaseHP:0040284 - Very rare23
HP:0000727HP:0000727Frontal lobe dementia0PINK1 CL E G H6501814581ORPHA:2828Young-onset Parkinson diseaseHP:0040284 - Very rare55
HP:0000727HP:0000727Frontal lobe dementia0PODXL CL E G H54209171ORPHA:2828Young-onset Parkinson diseaseHP:0040284 - Very rare6
HP:0000727HP:0000727Frontal lobe dementia0PRKN CL E G H50718607ORPHA:2828Young-onset Parkinson diseaseHP:0040284 - Very rare138
HP:0000727HP:0000727Frontal lobe dementia0PSEN1 CL E G H56639508OMIM:600274Frontotemporal dementia.241
HP:0000727HP:0000727Frontal lobe dementia0SNCA CL E G H662211138ORPHA:2828Young-onset Parkinson diseaseHP:0040284 - Very rare65
HP:0000727HP:0000727Frontal lobe dementia0SYNJ1 CL E G H886711503ORPHA:2828Young-onset Parkinson diseaseHP:0040284 - Very rare9
HP:0000727HP:0000727Frontal lobe dementia0TBP CL E G H690811588OMIM:607136Spinocerebellar ataxia 17.7
HP:0000727HP:0000727Frontal lobe dementia0TREM2 CL E G H5420917761ORPHA:2770Nasu-Hakola diseaseHP:0040281 - Very frequent31
HP:0000727HP:0000727Frontal lobe dementia0TYROBP CL E G H730512449ORPHA:2770Nasu-Hakola diseaseHP:0040281 - Very frequent22
HP:0000727HP:0000727Frontal lobe dementia0TYROBP CL E G H730512449OMIM:221770Polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy.22
HP:0000727HP:0000727Frontal lobe dementia0UCHL1 CL E G H734512513ORPHA:2828Young-onset Parkinson diseaseHP:0040284 - Very rare21
HP:0000727HP:0000727Frontal lobe dementia0VPS13C CL E G H5483223594ORPHA:2828Young-onset Parkinson diseaseHP:0040284 - Very rare8


Genes (19) :CHCHD10 CSF1R DNAJC6 FTL HTRA2 LRRK2 MAPT PARK7 PINK1 PODXL PRKN PSEN1 SNCA SYNJ1 TBP TREM2 TYROBP UCHL1 VPS13C

Diseases (8) :OMIM:615911 OMIM:221820 ORPHA:2828 ORPHA:157846 OMIM:600274 OMIM:607136 ORPHA:2770 OMIM:221770
 

Human Phenotype Ontology(HPO) is developed by the Human Phenotype Ontology Consortium. The version used here is December 15 2022 release.