Human Phenotype Ontology 
Grandparent Node:
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Cerebral atrophy (HP:0002059)help
Parent Node:
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Cerebral cortical atrophy (HP:0002120)help
..Starting node
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Temporal cortical atrophy (HP:0007112)help
Term ID: 7112
Name: Temporal cortical atrophy
Synonym:
Definition: Atrophy of the temporal cortex.
Comments:
Reference: HP:0007112
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandCerebral cortical hemiatrophy (HP:0100308) help
..expandFrontal cortical atrophy (HP:0006913) help
..expandOccipital cortical atrophy (HP:0012105) help
..expandParietal cortical atrophy (HP:0012104) help
InputHPO IDHPO termDistanceGeneGene id entrezDiseaseIdDiseaseNameDiseaseMIMConceptIDSourceTypical associationHGMD variantsClinVar variantsHGNC IDGeneMIM
 
HPO disease - gene - phenotype typical associations:
HP:0007112HP:0007112Temporal cortical atrophy0C9orf72 CL E G H203228100070ORPHA116528337614260
HP:0007112HP:0007112Temporal cortical atrophy0C9orf72 CL E G H203228100070ORPHA116128337614260
HP:0007112HP:0007112Temporal cortical atrophy0CHMP2B CL E G H25978100070ORPHA113024537609512
HP:0007112HP:0007112Temporal cortical atrophy0CHMP2B CL E G H25978100070ORPHA111024537609512
HP:0007112HP:0007112Temporal cortical atrophy0GRN CL E G H2896100070ORPHA13584601138945
HP:0007112HP:0007112Temporal cortical atrophy0GRN CL E G H2896100070ORPHA13024601138945
HP:0007112HP:0007112Temporal cortical atrophy0MAPT CL E G H4137100070ORPHA14886893157140
HP:0007112HP:0007112Temporal cortical atrophy0MAPT CL E G H4137100070ORPHA14656893157140
HP:0007112HP:0007112Temporal cortical atrophy0PSEN1 CL E G H5663100070ORPHA14319508104311
HP:0007112HP:0007112Temporal cortical atrophy0PSEN1 CL E G H5663100070ORPHA14089508104311
HP:0007112HP:0007112Temporal cortical atrophy0TMEM106B CL E G H54664100070ORPHA17422407613413
HP:0007112HP:0007112Temporal cortical atrophy0TMEM106B CL E G H54664100070ORPHA16222407613413
HP:0007112HP:0007112Temporal cortical atrophy0TREM2 CL E G H54209100070ORPHA19417761605086
HP:0007112HP:0007112Temporal cortical atrophy0TREM2 CL E G H54209100070ORPHA16417761605086
HP:0007112HP:0007112Temporal cortical atrophy0VCP CL E G H7415100070ORPHA139512666601023
HP:0007112HP:0007112Temporal cortical atrophy0VCP CL E G H7415100070ORPHA135612666601023
HP:0007112HP:0007112Temporal cortical atrophy0VCP CL E G H7415167320Inclusion body myopathy with early-onset paget disease and frontotemporal dementia167320C1833662OMIM139512666601023
HP:0007112HP:0007112Temporal cortical atrophy0VCP CL E G H7415167320Inclusion body myopathy with early-onset paget disease and frontotemporal dementia167320C1833662OMIM135612666601023
HP:0007112HP:0410170Hippocampal atrophy1C9orf72 CL E G H203228100070ORPHA116528337614260
HP:0007112HP:0410170Hippocampal atrophy1C9orf72 CL E G H203228100070ORPHA116128337614260
HP:0007112HP:0410170Hippocampal atrophy1CHMP2B CL E G H25978100070ORPHA113024537609512
HP:0007112HP:0410170Hippocampal atrophy1CHMP2B CL E G H25978100070ORPHA111024537609512
HP:0007112HP:0410170Hippocampal atrophy1GRN CL E G H2896100070ORPHA13584601138945
HP:0007112HP:0410170Hippocampal atrophy1GRN CL E G H2896100070ORPHA13024601138945
HP:0007112HP:0410170Hippocampal atrophy1MAPT CL E G H4137100070ORPHA14886893157140
HP:0007112HP:0410170Hippocampal atrophy1MAPT CL E G H4137100070ORPHA14656893157140
HP:0007112HP:0410170Hippocampal atrophy1PSEN1 CL E G H5663100070ORPHA14319508104311
HP:0007112HP:0410170Hippocampal atrophy1PSEN1 CL E G H5663100070ORPHA14089508104311
HP:0007112HP:0410170Hippocampal atrophy1TMEM106B CL E G H54664100070ORPHA17422407613413
HP:0007112HP:0410170Hippocampal atrophy1TMEM106B CL E G H54664100070ORPHA16222407613413
HP:0007112HP:0410170Hippocampal atrophy1TREM2 CL E G H54209100070ORPHA19417761605086
HP:0007112HP:0410170Hippocampal atrophy1TREM2 CL E G H54209100070ORPHA16417761605086
HP:0007112HP:0410170Hippocampal atrophy1VCP CL E G H7415100070ORPHA139512666601023
HP:0007112HP:0410170Hippocampal atrophy1VCP CL E G H7415100070ORPHA135612666601023
HP:0007112HP:0410170Hippocampal atrophy1VCP CL E G H7415167320Inclusion body myopathy with early-onset paget disease and frontotemporal dementia167320C1833662OMIM139512666601023
HP:0007112HP:0410170Hippocampal atrophy1VCP CL E G H7415167320Inclusion body myopathy with early-onset paget disease and frontotemporal dementia167320C1833662OMIM135612666601023
HP:0007112HP:0033715Hippocampal sclerosis2C9orf72 CL E G H203228100070ORPHA116528337614260
HP:0007112HP:0033715Hippocampal sclerosis2C9orf72 CL E G H203228100070ORPHA116128337614260
HP:0007112HP:0033715Hippocampal sclerosis2CHMP2B CL E G H25978100070ORPHA113024537609512
HP:0007112HP:0033715Hippocampal sclerosis2CHMP2B CL E G H25978100070ORPHA111024537609512
HP:0007112HP:0033715Hippocampal sclerosis2GRN CL E G H2896100070ORPHA13584601138945
HP:0007112HP:0033715Hippocampal sclerosis2GRN CL E G H2896100070ORPHA13024601138945
HP:0007112HP:0033715Hippocampal sclerosis2MAPT CL E G H4137100070ORPHA14886893157140
HP:0007112HP:0033715Hippocampal sclerosis2MAPT CL E G H4137100070ORPHA14656893157140
HP:0007112HP:0033715Hippocampal sclerosis2PSEN1 CL E G H5663100070ORPHA14319508104311
HP:0007112HP:0033715Hippocampal sclerosis2PSEN1 CL E G H5663100070ORPHA14089508104311
HP:0007112HP:0033715Hippocampal sclerosis2TMEM106B CL E G H54664100070ORPHA17422407613413
HP:0007112HP:0033715Hippocampal sclerosis2TMEM106B CL E G H54664100070ORPHA16222407613413
HP:0007112HP:0033715Hippocampal sclerosis2TREM2 CL E G H54209100070ORPHA19417761605086
HP:0007112HP:0033715Hippocampal sclerosis2TREM2 CL E G H54209100070ORPHA16417761605086
HP:0007112HP:0033715Hippocampal sclerosis2VCP CL E G H7415100070ORPHA139512666601023
HP:0007112HP:0033715Hippocampal sclerosis2VCP CL E G H7415100070ORPHA135612666601023
HP:0007112HP:0033715Hippocampal sclerosis2VCP CL E G H7415167320Inclusion body myopathy with early-onset paget disease and frontotemporal dementia167320C1833662OMIM139512666601023
HP:0007112HP:0033715Hippocampal sclerosis2VCP CL E G H7415167320Inclusion body myopathy with early-onset paget disease and frontotemporal dementia167320C1833662OMIM135612666601023
 
HPO disease - gene - phenotype less frequent non-typical associations:


Genes (11) :C9ORF72 C9orf72 CAMTA1 CHMP2B CPA6 GRN MAPT PSEN1 TMEM106B TREM2 VCP

Diseases (4) :100070 167320 614756 614418
 

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